{
    "disease_id": "DOID:0060308",
    "recommended_name": {
        "id": "DOID:0060308",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060308",
        "name": "autosomal recessive non-syndromic intellectual disability",
        "description": "A non-syndromic intellectual disability characterized by an autosomal recessive inheritance pattern."
    },
    "synonyms": [
        {
            "id": "DOID:0060308",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060308",
            "name": "autosomal recessive non-syndromic mental retardation",
            "description": ""
        },
        {
            "id": "DOID:0060308",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060308",
            "name": "autosomal recessive mental retardation",
            "description": ""
        },
        {
            "id": "MONDO:0009580",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009580",
            "name": "intellectual disability, autosomal recessive 1",
            "description": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the PRSS12 gene."
        },
        {
            "id": "MONDO:0009580",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009580",
            "name": "MRT1",
            "description": ""
        },
        {
            "id": "MONDO:0009580",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009580",
            "name": "mental retardation, autosomal recessive 1",
            "description": ""
        },
        {
            "id": "MONDO:0009580",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009580",
            "name": "autosomal recessive non-syndromic intellectual disability caused by mutation in PRSS12",
            "description": ""
        },
        {
            "id": "MONDO:0009580",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009580",
            "name": "mental retardation, autosomal recessive 1; MRT1",
            "description": ""
        },
        {
            "id": "MONDO:0009580",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009580",
            "name": "mental retardation, autosomal recessive type 1",
            "description": ""
        },
        {
            "id": "MONDO:0009580",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009580",
            "name": "PRSS12 autosomal recessive non-syndromic intellectual disability",
            "description": ""
        },
        {
            "id": "MONDO:0014210",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014210",
            "name": "intellectual disability-hypotonia-spasticity-sleep disorder syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0014210",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014210",
            "name": "mental retardation, autosomal recessive type 37",
            "description": ""
        },
        {
            "id": "MONDO:0014210",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014210",
            "name": "mental retardation, autosomal recessive 37",
            "description": ""
        },
        {
            "id": "MONDO:0014210",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014210",
            "name": "MRT37",
            "description": ""
        },
        {
            "id": "MONDO:0014210",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014210",
            "name": "mental retardation, autosomal recessive 37; MRT37",
            "description": ""
        },
        {
            "id": "MONDO:0014224",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014224",
            "name": "developmental delay with autism spectrum disorder and gait instability",
            "description": "Developmental delay with autism spectrum disorder and gait instability is a rare, genetic, neurological disorder characterized by infant hypotonia and feeding difficulties, global development delay, mild to moderated intellectual disability, delayed independent ambulation, broad-based gait with arms upheld and flexed at the elbow with brisk walking or running, and limited language skills. Behavior patterns are highly variable and range from sociable and affectionate to autistic behavior."
        },
        {
            "id": "MONDO:0014224",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014224",
            "name": "mental retardation, autosomal recessive 38",
            "description": ""
        },
        {
            "id": "MONDO:0014224",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014224",
            "name": "MRT38",
            "description": ""
        },
        {
            "id": "MONDO:0014224",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014224",
            "name": "mental retardation, autosomal recessive 38; MRT38",
            "description": ""
        },
        {
            "id": "MONDO:0014224",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014224",
            "name": "developmental delay with ASD and gait instability",
            "description": ""
        },
        {
            "id": "MONDO:0014224",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014224",
            "name": "mental retardation, autosomal recessive type 38",
            "description": ""
        },
        {
            "id": "MONDO:0013528",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013528",
            "name": "intellectual disability, autosomal recessive 14",
            "description": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the TECR gene."
        },
        {
            "id": "MONDO:0013528",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013528",
            "name": "mental retardation, autosomal recessive 14",
            "description": ""
        },
        {
            "id": "MONDO:0013528",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013528",
            "name": "autosomal recessive non-syndromic intellectual disability caused by mutation in TECR",
            "description": ""
        },
        {
            "id": "MONDO:0013528",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013528",
            "name": "MRT14",
            "description": ""
        },
        {
            "id": "MONDO:0013528",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013528",
            "name": "mental retardation, autosomal recessive 14; MRT14",
            "description": ""
        },
        {
            "id": "MONDO:0013528",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013528",
            "name": "TECR autosomal recessive non-syndromic intellectual disability",
            "description": ""
        },
        {
            "id": "MONDO:0013528",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013528",
            "name": "mental retardation, autosomal recessive type 14",
            "description": ""
        },
        {
            "id": "MONDO:0014273",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014273",
            "name": "microcephaly-thin corpus callosum-intellectual disability syndrome",
            "description": "Microcephaly-thin corpus callosum-intellectual disability syndrome is a rare, genetic, syndromic intellectual disability disease characterized by progressive postnatal microcephaly and global developmental delay, as well as moderate to profound intellectual disability, difficulty or inability to walk, pyramidal signs (including spasticity, hyperreflexia and extensor plantar response) and thin corpus callosum revealed by brain imaging. Ophthalmologic signs (including nystagmus, strabismus and abnormal retinal pigmentation), foot deformity and genital anomalies may also be associated."
        },
        {
            "id": "MONDO:0014273",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014273",
            "name": "mental retardation, autosomal recessive type 40",
            "description": ""
        },
        {
            "id": "MONDO:0014273",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014273",
            "name": "mental retardation, autosomal recessive 40; MRT40",
            "description": ""
        },
        {
            "id": "MONDO:0014273",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014273",
            "name": "mental retardation, autosomal recessive 40",
            "description": ""
        },
        {
            "id": "MONDO:0014273",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014273",
            "name": "MRT40",
            "description": ""
        },
        {
            "id": "MONDO:0013697",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013697",
            "name": "MRT29",
            "description": ""
        },
        {
            "id": "MONDO:0013697",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013697",
            "name": "mental retardation, autosomal recessive 29; MRT29",
            "description": ""
        },
        {
            "id": "MONDO:0013697",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013697",
            "name": "MRT29",
            "description": ""
        },
        {
            "id": "MONDO:0013697",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013697",
            "name": "mental retardation, autosomal recessive 29",
            "description": ""
        },
        {
            "id": "MONDO:0014348",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014348",
            "name": "intellectual disability, autosomal recessive 42",
            "description": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the PGAP1 gene."
        },
        {
            "id": "MONDO:0014348",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014348",
            "name": "mental retardation, autosomal recessive type 42",
            "description": ""
        },
        {
            "id": "MONDO:0014348",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014348",
            "name": "PGAP1 autosomal recessive non-syndromic intellectual disability",
            "description": ""
        },
        {
            "id": "MONDO:0014348",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014348",
            "name": "glycosylphosphatidylinositol biosynthesis defect 9",
            "description": ""
        },
        {
            "id": "MONDO:0014348",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014348",
            "name": "mental retardation, autosomal recessive 42; MRT42",
            "description": ""
        },
        {
            "id": "MONDO:0014348",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014348",
            "name": "autosomal recessive non-syndromic intellectual disability caused by mutation in PGAP1",
            "description": ""
        },
        {
            "id": "MONDO:0014348",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014348",
            "name": "mental retardation, autosomal recessive 42",
            "description": ""
        },
        {
            "id": "MONDO:0014348",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014348",
            "name": "MRT42",
            "description": ""
        },
        {
            "id": "MONDO:0012037",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012037",
            "name": "intellectual disability, autosomal recessive 3",
            "description": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the CC2D1A gene."
        },
        {
            "id": "MONDO:0012037",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012037",
            "name": "autosomal recessive non-syndromic intellectual disability caused by mutation in CC2D1A",
            "description": ""
        },
        {
            "id": "MONDO:0012037",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012037",
            "name": "MRT3",
            "description": ""
        },
        {
            "id": "MONDO:0012037",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012037",
            "name": "mental retardation, autosomal recessive 3",
            "description": ""
        },
        {
            "id": "MONDO:0012037",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012037",
            "name": "mental retardation, autosomal recessive 3; MRT3",
            "description": ""
        },
        {
            "id": "MONDO:0012037",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012037",
            "name": "CC2D1A autosomal recessive non-syndromic intellectual disability",
            "description": ""
        },
        {
            "id": "MONDO:0012037",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012037",
            "name": "mental retardation, autosomal recessive type 3",
            "description": ""
        },
        {
            "id": "MONDO:0014289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014289",
            "name": "macrocephaly-developmental delay syndrome",
            "description": "Macrocephaly-developmental delay syndrome is a rare, intellectual disability syndrome characterized by macrocephaly, mild dysmorphic features (frontal bossing, long face, hooded eye lids with small, downslanting palpebral fissures, broad nasal bridge, and prominent chin), global neurodevelopmental delay, behavioral abnormalities (e.g. anxiety, stereotyped movements) and absence or generalized tonic-clonic seizures. Additional features reported in some patients include craniosynostosis, fifth finger clinodactyly, recurrent pneumonia, and hepatosplenomegally."
        },
        {
            "id": "MONDO:0014289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014289",
            "name": "mental retardation, autosomal recessive 41",
            "description": ""
        },
        {
            "id": "MONDO:0014289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014289",
            "name": "MRT41",
            "description": ""
        },
        {
            "id": "MONDO:0014289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014289",
            "name": "mental retardation, autosomal recessive type 41",
            "description": ""
        },
        {
            "id": "MONDO:0014289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014289",
            "name": "mental retardation, autosomal recessive 41; MRT41",
            "description": ""
        },
        {
            "id": "MONDO:0013694",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013694",
            "name": "MRT31",
            "description": ""
        },
        {
            "id": "MONDO:0013694",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013694",
            "name": "MRT31",
            "description": ""
        },
        {
            "id": "MONDO:0013694",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013694",
            "name": "mental retardation, autosomal recessive 31; MRT31",
            "description": ""
        },
        {
            "id": "MONDO:0013694",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013694",
            "name": "mental retardation, autosomal recessive 31",
            "description": ""
        },
        {
            "id": "MONDO:0014409",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014409",
            "name": "intellectual disability, autosomal recessive 44",
            "description": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the METTL23 gene."
        },
        {
            "id": "MONDO:0014409",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014409",
            "name": "mental retardation, autosomal recessive type 44",
            "description": ""
        },
        {
            "id": "MONDO:0014409",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014409",
            "name": "autosomal recessive non-syndromic intellectual disability caused by mutation in METTL23",
            "description": ""
        },
        {
            "id": "MONDO:0014409",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014409",
            "name": "mental retardation, autosomal recessive 44; MRT44",
            "description": ""
        },
        {
            "id": "MONDO:0014409",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014409",
            "name": "mental retardation, autosomal recessive 44",
            "description": ""
        },
        {
            "id": "MONDO:0014409",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014409",
            "name": "MRT44",
            "description": ""
        },
        {
            "id": "MONDO:0014409",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014409",
            "name": "METTL23 autosomal recessive non-syndromic intellectual disability",
            "description": ""
        },
        {
            "id": "MONDO:0012623",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012623",
            "name": "MRT4",
            "description": ""
        },
        {
            "id": "MONDO:0012623",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012623",
            "name": "MRT4",
            "description": ""
        },
        {
            "id": "MONDO:0012623",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012623",
            "name": "mental retardation, autosomal recessive 4",
            "description": ""
        },
        {
            "id": "MONDO:0012623",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012623",
            "name": "mental retardation, autosomal recessive 4; MRT4",
            "description": ""
        },
        {
            "id": "MONDO:0011828",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011828",
            "name": "intellectual disability, autosomal recessive 2",
            "description": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the CRBN gene."
        },
        {
            "id": "MONDO:0011828",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011828",
            "name": "mental retardation, autosomal recessive 2; MRT2",
            "description": ""
        },
        {
            "id": "MONDO:0011828",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011828",
            "name": "CRBN autosomal recessive non-syndromic intellectual disability",
            "description": ""
        },
        {
            "id": "MONDO:0011828",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011828",
            "name": "mental retardation, autosomal recessive type 2",
            "description": ""
        },
        {
            "id": "MONDO:0011828",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011828",
            "name": "autosomal recessive non-syndromic intellectual disability caused by mutation in CRBN",
            "description": ""
        },
        {
            "id": "MONDO:0011828",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011828",
            "name": "mental retardation, autosomal recessive 2A",
            "description": ""
        },
        {
            "id": "MONDO:0011828",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011828",
            "name": "MRT2",
            "description": ""
        },
        {
            "id": "MONDO:0011828",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011828",
            "name": "mental retardation, autosomal recessive 2",
            "description": ""
        },
        {
            "id": "MONDO:0013708",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013708",
            "name": "MRT25",
            "description": ""
        },
        {
            "id": "MONDO:0013708",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013708",
            "name": "MRT25",
            "description": ""
        },
        {
            "id": "MONDO:0013708",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013708",
            "name": "mental retardation, autosomal recessive 25",
            "description": ""
        },
        {
            "id": "MONDO:0013708",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013708",
            "name": "mental retardation, autosomal recessive 25; MRT25",
            "description": ""
        },
        {
            "id": "MONDO:0013709",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013709",
            "name": "MRT28",
            "description": ""
        },
        {
            "id": "MONDO:0013709",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013709",
            "name": "MRT28",
            "description": ""
        },
        {
            "id": "MONDO:0013709",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013709",
            "name": "mental retardation, autosomal recessive 28",
            "description": ""
        },
        {
            "id": "MONDO:0013709",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013709",
            "name": "mental retardation, autosomal recessive 28; MRT28",
            "description": ""
        },
        {
            "id": "MONDO:0013706",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013706",
            "name": "MRT23",
            "description": ""
        },
        {
            "id": "MONDO:0013706",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013706",
            "name": "MRT23",
            "description": ""
        },
        {
            "id": "MONDO:0013706",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013706",
            "name": "mental retardation, autosomal recessive 23",
            "description": ""
        },
        {
            "id": "MONDO:0013706",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013706",
            "name": "mental retardation, autosomal recessive 23; MRT23",
            "description": ""
        },
        {
            "id": "MONDO:0013707",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013707",
            "name": "MRT24",
            "description": ""
        },
        {
            "id": "MONDO:0013707",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013707",
            "name": "MRT24",
            "description": ""
        },
        {
            "id": "MONDO:0013707",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013707",
            "name": "mental retardation, autosomal recessive 24",
            "description": ""
        },
        {
            "id": "MONDO:0013707",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013707",
            "name": "mental retardation, autosomal recessive 24; MRT24",
            "description": ""
        },
        {
            "id": "MONDO:0013704",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013704",
            "name": "MRT30",
            "description": ""
        },
        {
            "id": "MONDO:0013704",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013704",
            "name": "MRT30",
            "description": ""
        },
        {
            "id": "MONDO:0013704",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013704",
            "name": "mental retardation, autosomal recessive 30; MRT30",
            "description": ""
        },
        {
            "id": "MONDO:0013704",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013704",
            "name": "mental retardation, autosomal recessive 30",
            "description": ""
        },
        {
            "id": "MONDO:0013705",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013705",
            "name": "MRT19",
            "description": ""
        },
        {
            "id": "MONDO:0013705",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013705",
            "name": "mental retardation, autosomal recessive 19; MRT19",
            "description": ""
        },
        {
            "id": "MONDO:0013705",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013705",
            "name": "MRT19",
            "description": ""
        },
        {
            "id": "MONDO:0013705",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013705",
            "name": "mental retardation, autosomal recessive 19",
            "description": ""
        },
        {
            "id": "MONDO:0013702",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013702",
            "name": "intellectual disability, autosomal recessive 27",
            "description": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the LINS1 gene."
        },
        {
            "id": "MONDO:0013702",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013702",
            "name": "mental retardation, autosomal recessive 27; MRT27",
            "description": ""
        },
        {
            "id": "MONDO:0013702",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013702",
            "name": "LINS1 autosomal recessive non-syndromic intellectual disability",
            "description": ""
        },
        {
            "id": "MONDO:0013702",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013702",
            "name": "mental retardation, autosomal recessive type 27",
            "description": ""
        },
        {
            "id": "MONDO:0013702",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013702",
            "name": "autosomal recessive non-syndromic intellectual disability caused by mutation in LINS1",
            "description": ""
        },
        {
            "id": "MONDO:0013702",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013702",
            "name": "mental retardation, autosomal recessive 27",
            "description": ""
        },
        {
            "id": "MONDO:0013702",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013702",
            "name": "MRT27",
            "description": ""
        },
        {
            "id": "MONDO:0013703",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013703",
            "name": "MRT33",
            "description": ""
        },
        {
            "id": "MONDO:0013703",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013703",
            "name": "MRT33",
            "description": ""
        },
        {
            "id": "MONDO:0013703",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013703",
            "name": "mental retardation, autosomal recessive 33",
            "description": ""
        },
        {
            "id": "MONDO:0013703",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013703",
            "name": "mental retardation, autosomal recessive 33; MRT33",
            "description": ""
        },
        {
            "id": "MONDO:0012617",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012617",
            "name": "MRT9",
            "description": ""
        },
        {
            "id": "MONDO:0012617",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012617",
            "name": "MRT9",
            "description": ""
        },
        {
            "id": "MONDO:0012617",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012617",
            "name": "mental retardation, autosomal recessive 9; MRT9",
            "description": ""
        },
        {
            "id": "MONDO:0012617",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012617",
            "name": "mental retardation, autosomal recessive 26",
            "description": ""
        },
        {
            "id": "MONDO:0012617",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012617",
            "name": "mental retardation, autosomal recessive 9",
            "description": ""
        },
        {
            "id": "MONDO:0012619",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012619",
            "name": "MRT11",
            "description": ""
        },
        {
            "id": "MONDO:0012619",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012619",
            "name": "MRT11",
            "description": ""
        },
        {
            "id": "MONDO:0012619",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012619",
            "name": "mental retardation, autosomal recessive 11",
            "description": ""
        },
        {
            "id": "MONDO:0012619",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012619",
            "name": "mental retardation, autosomal recessive 11; MRT11",
            "description": ""
        },
        {
            "id": "MONDO:0012613",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012613",
            "name": "intellectual disability, autosomal recessive 5",
            "description": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the NSUN2 gene."
        },
        {
            "id": "MONDO:0012613",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012613",
            "name": "mental retardation, autosomal recessive type 5",
            "description": ""
        },
        {
            "id": "MONDO:0012613",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012613",
            "name": "NSUN2 autosomal recessive non-syndromic intellectual disability",
            "description": ""
        },
        {
            "id": "MONDO:0012613",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012613",
            "name": "autosomal recessive non-syndromic intellectual disability caused by mutation in NSUN2",
            "description": ""
        },
        {
            "id": "MONDO:0012613",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012613",
            "name": "mental retardation, autosomal recessive 5; MRT5",
            "description": ""
        },
        {
            "id": "MONDO:0012613",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012613",
            "name": "MRT5",
            "description": ""
        },
        {
            "id": "MONDO:0012613",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012613",
            "name": "mental retardation, autosomal recessive 5",
            "description": ""
        },
        {
            "id": "MONDO:0012612",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012612",
            "name": "intellectual disability, autosomal recessive 12",
            "description": ""
        },
        {
            "id": "MONDO:0012612",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012612",
            "name": "mental retardation, autosomal recessive 12",
            "description": ""
        },
        {
            "id": "MONDO:0012612",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012612",
            "name": "MRT12",
            "description": ""
        },
        {
            "id": "MONDO:0012612",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012612",
            "name": "mental retardation, autosomal recessive 12; MRT12",
            "description": ""
        },
        {
            "id": "MONDO:0012612",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012612",
            "name": "mental retardation, autosomal recessive type 12",
            "description": ""
        },
        {
            "id": "MONDO:0012615",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012615",
            "name": "intellectual disability, autosomal recessive 7",
            "description": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the TUSC3 gene."
        },
        {
            "id": "MONDO:0012615",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012615",
            "name": "mental retardation, autosomal recessive 22",
            "description": ""
        },
        {
            "id": "MONDO:0012615",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012615",
            "name": "mental retardation, autosomal recessive type 7",
            "description": ""
        },
        {
            "id": "MONDO:0012615",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012615",
            "name": "TUSC3 autosomal recessive non-syndromic intellectual disability",
            "description": ""
        },
        {
            "id": "MONDO:0012615",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012615",
            "name": "mental retardation, autosomal recessive 7; MRT7",
            "description": ""
        },
        {
            "id": "MONDO:0012615",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012615",
            "name": "MRT7",
            "description": ""
        },
        {
            "id": "MONDO:0012615",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012615",
            "name": "autosomal recessive non-syndromic intellectual disability caused by mutation in TUSC3",
            "description": ""
        },
        {
            "id": "MONDO:0012615",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012615",
            "name": "mental retardation, autosomal recessive 7",
            "description": ""
        },
        {
            "id": "MONDO:0014238",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014238",
            "name": "severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0014238",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014238",
            "name": "mental retardation, autosomal recessive 39; MRT39",
            "description": ""
        },
        {
            "id": "MONDO:0014238",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014238",
            "name": "mental retardation, autosomal recessive type 39",
            "description": ""
        },
        {
            "id": "MONDO:0014238",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014238",
            "name": "mental retardation, autosomal recessive 39",
            "description": ""
        },
        {
            "id": "MONDO:0014238",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014238",
            "name": "MRT39",
            "description": ""
        },
        {
            "id": "MONDO:0014354",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014354",
            "name": "intellectual disability, autosomal recessive 43",
            "description": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the WASHC4 gene."
        },
        {
            "id": "MONDO:0014354",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014354",
            "name": "WASHC4 autosomal recessive non-syndromic intellectual disability",
            "description": ""
        },
        {
            "id": "MONDO:0014354",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014354",
            "name": "mental retardation, autosomal recessive type 43",
            "description": ""
        },
        {
            "id": "MONDO:0014354",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014354",
            "name": "autosomal recessive non-syndromic intellectual disability caused by mutation in WASHC4",
            "description": ""
        },
        {
            "id": "MONDO:0014354",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014354",
            "name": "mental retardation, autosomal recessive 43",
            "description": ""
        },
        {
            "id": "MONDO:0014354",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014354",
            "name": "mental retardation, autosomal recessive 43; MRT43",
            "description": ""
        },
        {
            "id": "MONDO:0014354",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014354",
            "name": "MRT43",
            "description": ""
        },
        {
            "id": "MONDO:0013785",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013785",
            "name": "intellectual disability, autosomal recessive 34",
            "description": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the CRADD gene."
        },
        {
            "id": "MONDO:0013785",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013785",
            "name": "mental retardation, autosomal recessive type 34",
            "description": ""
        },
        {
            "id": "MONDO:0013785",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013785",
            "name": "mental retardation, autosomal recessive 34, with variant lissencephaly",
            "description": ""
        },
        {
            "id": "MONDO:0013785",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013785",
            "name": "CRADD autosomal recessive non-syndromic intellectual disability",
            "description": ""
        },
        {
            "id": "MONDO:0013785",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013785",
            "name": "mental retardation, autosomal recessive 34, with variant lissencephaly; MRT34",
            "description": ""
        },
        {
            "id": "MONDO:0013785",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013785",
            "name": "mental retardation, autosomal recessive 34",
            "description": ""
        },
        {
            "id": "MONDO:0013785",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013785",
            "name": "MRT34",
            "description": ""
        },
        {
            "id": "MONDO:0013785",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013785",
            "name": "mental retardation, autosomal recessive 34; MRT34",
            "description": ""
        },
        {
            "id": "MONDO:0013785",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013785",
            "name": "autosomal recessive non-syndromic intellectual disability caused by mutation in CRADD",
            "description": ""
        },
        {
            "id": "MONDO:0013651",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013651",
            "name": "intellectual disability, autosomal recessive 18",
            "description": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the MED23 gene."
        },
        {
            "id": "MONDO:0013651",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013651",
            "name": "mental retardation, autosomal recessive type 18",
            "description": ""
        },
        {
            "id": "MONDO:0013651",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013651",
            "name": "mental retardation, autosomal recessive 18",
            "description": ""
        },
        {
            "id": "MONDO:0013651",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013651",
            "name": "MED23",
            "description": ""
        },
        {
            "id": "MONDO:0013651",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013651",
            "name": "MRT18",
            "description": ""
        },
        {
            "id": "MONDO:0013651",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013651",
            "name": "MED23 autosomal recessive non-syndromic intellectual disability",
            "description": ""
        },
        {
            "id": "MONDO:0013651",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013651",
            "name": "autosomal recessive nonsyndromic mental retardation-18",
            "description": ""
        },
        {
            "id": "MONDO:0013651",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013651",
            "name": "mental retardation, autosomal recessive 18; MRT18",
            "description": ""
        },
        {
            "id": "MONDO:0013651",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013651",
            "name": "autosomal recessive non-syndromic intellectual disability caused by mutation in MED23",
            "description": ""
        },
        {
            "id": "MONDO:0012618",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012618",
            "name": "MRT10",
            "description": ""
        },
        {
            "id": "MONDO:0012618",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012618",
            "name": "mental retardation, autosomal recessive 20",
            "description": ""
        },
        {
            "id": "MONDO:0012618",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012618",
            "name": "MRT10",
            "description": ""
        },
        {
            "id": "MONDO:0012618",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012618",
            "name": "mental retardation, autosomal recessive 10; MRT10",
            "description": ""
        },
        {
            "id": "MONDO:0012618",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012618",
            "name": "mental retardation, autosomal recessive 10",
            "description": ""
        },
        {
            "id": "MONDO:0012614",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012614",
            "name": "intellectual disability, autosomal recessive 6",
            "description": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the GRIK2 gene."
        },
        {
            "id": "MONDO:0012614",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012614",
            "name": "GRIK2 autosomal recessive non-syndromic intellectual disability",
            "description": ""
        },
        {
            "id": "MONDO:0012614",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012614",
            "name": "mental retardation, autosomal recessive type 6",
            "description": ""
        },
        {
            "id": "MONDO:0012614",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012614",
            "name": "autosomal recessive non-syndromic intellectual disability caused by mutation in GRIK2",
            "description": ""
        },
        {
            "id": "MONDO:0012614",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012614",
            "name": "mental retardation, autosomal recessive 6; MRT6",
            "description": ""
        },
        {
            "id": "MONDO:0012614",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012614",
            "name": "MRT6",
            "description": ""
        },
        {
            "id": "MONDO:0012614",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012614",
            "name": "mental retardation, autosomal recessive 6",
            "description": ""
        },
        {
            "id": "MONDO:0013629",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013629",
            "name": "MRT16",
            "description": ""
        },
        {
            "id": "MONDO:0013629",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013629",
            "name": "MRT16",
            "description": ""
        },
        {
            "id": "MONDO:0013629",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013629",
            "name": "mental retardation, autosomal recessive 16",
            "description": ""
        },
        {
            "id": "MONDO:0013629",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013629",
            "name": "mental retardation, autosomal recessive 16; MRT16",
            "description": ""
        },
        {
            "id": "MIM:249500",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/249500",
            "name": "Intellectual developmental disorder, autosomal recessive 1",
            "description": "Intellectual developmental disorder, autosomal recessive 1"
        },
        {
            "id": "MIM:615493",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615493",
            "name": "Intellectual developmental disorder, autosomal recessive 37",
            "description": "Intellectual developmental disorder, autosomal recessive 37"
        },
        {
            "id": "MIM:615516",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615516",
            "name": "Intellectual developmental disorder, autosomal recessive 38",
            "description": "Intellectual developmental disorder, autosomal recessive 38"
        },
        {
            "id": "MIM:614020",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614020",
            "name": "Intellectual developmental disorder, autosomal recessive 14",
            "description": "Intellectual developmental disorder, autosomal recessive 14"
        },
        {
            "id": "MIM:615599",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615599",
            "name": "Neurodevelopmental disorder with feeding difficulties, thin corpus callosum, and foot deformity",
            "description": "Neurodevelopmental disorder with feeding difficulties, thin corpus callosum, and foot deformity"
        },
        {
            "id": "MIM:615802",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615802",
            "name": "Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities",
            "description": "Neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities"
        },
        {
            "id": "MIM:608443",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/608443",
            "name": "Intellectual developmental disorder, autosomal recessive 3",
            "description": "Intellectual developmental disorder, autosomal recessive 3"
        },
        {
            "id": "MIM:615637",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615637",
            "name": "Intellectual developmental disorder, autosomal recessive 41",
            "description": "Intellectual developmental disorder, autosomal recessive 41"
        },
        {
            "id": "MIM:615942",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615942",
            "name": "Intellectual developmental disorder, autosomal recessive 44",
            "description": "Intellectual developmental disorder, autosomal recessive 44"
        },
        {
            "id": "MIM:607417",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/607417",
            "name": "Intellectual developmental disorder, autosomal recessive 2",
            "description": "Intellectual developmental disorder, autosomal recessive 2"
        },
        {
            "id": "MIM:614340",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614340",
            "name": "Intellectual developmental disorder, autosomal recessive 27",
            "description": "Intellectual developmental disorder, autosomal recessive 27"
        },
        {
            "id": "MIM:611091",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/611091",
            "name": "Intellectual developmental disorder, autosomal recessive 5",
            "description": "Intellectual developmental disorder, autosomal recessive 5"
        },
        {
            "id": "MIM:611090",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/611090",
            "name": "Intellectual developmental disorder, autosomal recessive 12",
            "description": "Intellectual developmental disorder, autosomal recessive 12"
        },
        {
            "id": "MIM:611093",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/611093",
            "name": "Intellectual developmental disorder, autosomal recessive 7",
            "description": "Intellectual developmental disorder, autosomal recessive 7"
        },
        {
            "id": "MIM:615541",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615541",
            "name": "Intellectual developmental disorder, autosomal recessive 39",
            "description": "Intellectual developmental disorder, autosomal recessive 39"
        },
        {
            "id": "MIM:615817",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615817",
            "name": "Intellectual developmental disorder, autosomal recessive 43",
            "description": "Intellectual developmental disorder, autosomal recessive 43"
        },
        {
            "id": "MIM:614499",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614499",
            "name": "Intellectual developmental disorder, autosomal recessive 34, with variant lissencephaly",
            "description": "Intellectual developmental disorder, autosomal recessive 34, with variant lissencephaly"
        },
        {
            "id": "MIM:614249",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614249",
            "name": "Intellectual developmental disorder, autosomal recessive 18, with or without epilepsy",
            "description": "Intellectual developmental disorder, autosomal recessive 18, with or without epilepsy"
        },
        {
            "id": "MIM:611092",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/611092",
            "name": "Intellectual developmental disorder, autosomal recessive 6",
            "description": "Intellectual developmental disorder, autosomal recessive 6"
        }
    ]
}