{
    "disease_id": "DOID:0060179",
    "recommended_name": {
        "id": "DOID:0060179",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060179",
        "name": "Renpenning syndrome",
        "description": "An intellectual disability that is characterized by small head size (microcephaly), long narrow face, short stature, small testes, and intellectual deficit which follows X-linked inheritance and presents most often in males."
    },
    "synonyms": [
        {
            "id": "DOID:0060179",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060179",
            "name": "Golabi-Ito-Hall syndrome",
            "description": ""
        },
        {
            "id": "DOID:0060179",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060179",
            "name": "X-linked intellectual disability, Renpenning type",
            "description": ""
        },
        {
            "id": "DOID:0060179",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060179",
            "name": "X-linked mental retardation Renpenning type",
            "description": ""
        },
        {
            "id": "DOID:0060179",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060179",
            "name": "X-linked mental retardation with spastic diplegia",
            "description": ""
        },
        {
            "id": "DOID:0060179",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060179",
            "name": "syndromic X-linked mental retardation 8",
            "description": ""
        },
        {
            "id": "DOID:0060179",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060179",
            "name": "X-linked intellectual disability due to PQBP1 mutations",
            "description": ""
        },
        {
            "id": "DOID:0060179",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060179",
            "name": "Sutherland-Haan X-linked mental retardation syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010653",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010653",
            "name": "Renpenning syndrome",
            "description": "An X-linked syndrome characterized by intellectual deficiency, microcephaly, leanness and mild short stature."
        },
        {
            "id": "MONDO:0010653",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010653",
            "name": "Golabi-Ito-Hall syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010653",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010653",
            "name": "Renpenning syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010653",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010653",
            "name": "Renpenning syndrome type 1",
            "description": ""
        },
        {
            "id": "MONDO:0010653",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010653",
            "name": "Sutherland-Haan X-linked intellectual disability syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010653",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010653",
            "name": "Sutherland-Haan X-linked mental retardation syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010653",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010653",
            "name": "X-linked intellectual disability Renpenning type",
            "description": ""
        },
        {
            "id": "MONDO:0010653",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010653",
            "name": "X-linked intellectual disability due to PQBP1 mutations",
            "description": ""
        },
        {
            "id": "MONDO:0010653",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010653",
            "name": "X-linked intellectual disability with spastic diplegia",
            "description": ""
        },
        {
            "id": "MONDO:0010653",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010653",
            "name": "X-linked intellectual disability, Renpenning type",
            "description": ""
        },
        {
            "id": "MONDO:0010653",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010653",
            "name": "renpenning syndrome, X-linked recessive",
            "description": ""
        },
        {
            "id": "MONDO:0010653",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010653",
            "name": "syndromic X-linked intellectual disability 8",
            "description": ""
        },
        {
            "id": "MONDO:0010653",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010653",
            "name": "MRXS3",
            "description": ""
        },
        {
            "id": "MONDO:0010653",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010653",
            "name": "MRXS8",
            "description": ""
        },
        {
            "id": "MONDO:0010653",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010653",
            "name": "RENS1",
            "description": ""
        },
        {
            "id": "MONDO:0010653",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010653",
            "name": "Renpenning syndrome 1",
            "description": ""
        },
        {
            "id": "MONDO:0010653",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010653",
            "name": "Sutherland-Haan syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010653",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010653",
            "name": "X-linked intellectual disability syndromic 3",
            "description": ""
        },
        {
            "id": "MONDO:0010653",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010653",
            "name": "X-linked mental retardation syndromic 3",
            "description": ""
        },
        {
            "id": "MONDO:0010653",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010653",
            "name": "intellectual disability, X-linked Renpenning type",
            "description": ""
        },
        {
            "id": "MONDO:0010653",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010653",
            "name": "mental retardation, X-linked 55",
            "description": ""
        },
        {
            "id": "MONDO:0010653",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010653",
            "name": "mental retardation, X-linked Renpenning type",
            "description": ""
        },
        {
            "id": "MONDO:0010653",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010653",
            "name": "mental retardation, X-linked, Renpenning type",
            "description": ""
        },
        {
            "id": "MONDO:0010653",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010653",
            "name": "mental retardation, X-linked, syndromic 3",
            "description": ""
        },
        {
            "id": "MONDO:0010653",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010653",
            "name": "mental retardation, X-linked, syndromic 8",
            "description": ""
        },
        {
            "id": "MONDO:0010653",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010653",
            "name": "mental retardation, X-linked, with spastic diplegia",
            "description": ""
        },
        {
            "id": "MIM:309500",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/309500",
            "name": "Renpenning syndrome 1",
            "description": "Renpenning syndrome 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060179"
    ],
    "unlinked_id_list": []
}