{
    "disease_id": "DOID:0070067",
    "recommended_name": {
        "id": "DOID:0070067",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070067",
        "name": "White-Sutton syndrome",
        "description": "An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the POGZ gene on chromosome 1q21.3."
    },
    "synonyms": [
        {
            "id": "DOID:0070067",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070067",
            "name": "MRD37",
            "description": ""
        },
        {
            "id": "DOID:0070067",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070067",
            "name": "WHSUS",
            "description": ""
        },
        {
            "id": "DOID:0070067",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070067",
            "name": "autosomal dominant mental retardation 37",
            "description": ""
        },
        {
            "id": "MONDO:0014606",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014606",
            "name": "intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome",
            "description": "Intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome is a rare, genetic, syndromic intellectual disability disorder characterized by craniofacial dysmorphism (microcephaly, hypotonic facies, strabismus, long and flat malar region, posteriorly rotated ears, flat nasal bridge with broad nasal tip, short philtrum, thin vermillion border, open mouth with down-turned corners, high arched palate, pointed chin), global developmental delay, intellectual disability and variable neurobehavioral abnormalities (autism spectrum disorder, aggressiveness, self injury). Additional features include vision abnormalities and variable sensorineural hearing loss, as well as short stature, hypotonia and gastrointestinal manifestations (e.g. poor feeding, gastroesophageal reflux, constipation)."
        },
        {
            "id": "MONDO:0014606",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014606",
            "name": "MRD37",
            "description": ""
        },
        {
            "id": "MONDO:0014606",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014606",
            "name": "WHSUS",
            "description": ""
        },
        {
            "id": "MONDO:0014606",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014606",
            "name": "autosomal dominant intellectual disability 37",
            "description": ""
        },
        {
            "id": "MONDO:0014606",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014606",
            "name": "intellectual disability, autosomal dominant type 37",
            "description": ""
        },
        {
            "id": "MONDO:0014606",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014606",
            "name": "intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0014606",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014606",
            "name": "mental retardation, autosomal dominant type 37",
            "description": ""
        },
        {
            "id": "MONDO:0014606",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014606",
            "name": "intellectual disability, autosomal dominant 37",
            "description": ""
        },
        {
            "id": "MONDO:0014606",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014606",
            "name": "mental retardation, autosomal dominant 37",
            "description": ""
        },
        {
            "id": "MIM:616364",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616364",
            "name": "White-Sutton syndrome",
            "description": "White-Sutton syndrome"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070067"
    ],
    "unlinked_id_list": []
}