{
    "disease_id": "DOID:0060308", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014348", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014348", 
            "name": "intellectual disability, autosomal recessive 42"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014348", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014348", 
            "name": "mental retardation, autosomal recessive type 42"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014348", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014348", 
            "name": "PGAP1 autosomal recessive non-syndromic intellectual disability"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014348", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014348", 
            "name": "glycosylphosphatidylinositol biosynthesis defect 9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014348", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014348", 
            "name": "mental retardation, autosomal recessive 42; MRT42"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014348", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014348", 
            "name": "autosomal recessive non-syndromic intellectual disability caused by mutation in PGAP1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014348", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014348", 
            "name": "mental retardation, autosomal recessive 42"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014348", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014348", 
            "name": "MRT42"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060308", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060308", 
            "name": "autosomal recessive non-syndromic mental retardation"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060308", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060308", 
            "name": "autosomal recessive mental retardation"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060308", 
        "description": "A non-syndromic intellectual disability characterized by an autosomal recessive inheritance pattern.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060308", 
        "name": "autosomal recessive non-syndromic intellectual disability"
    }, 
    "evidence": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014348", 
            "id": "0014348", 
            "database": "MONDO"
        }, 
        {
            "url": "https://www.omim.org/entry/615802", 
            "id": "615802", 
            "database": "MIM"
        }
    ]
}