{
    "disease_id": "DOID:0060823",
    "recommended_name": {
        "id": "DOID:0060823",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060823",
        "name": "syndromic X-linked intellectual disability 94",
        "description": "A syndromic X-linked intellectual disability characterized by moderate intellectual disability with variable occurrence of asthenic body habitus, dysmorphic features, autistic features, macrocephaly, seizures, myoclonic jerks, and hyporeflexia that has_material_basis_in mutation in the GRIA3 gene on chromosome Xq25."
    },
    "synonyms": [
        {
            "id": "DOID:0060823",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060823",
            "name": "syndromic X-linked intellectual disability due to GRIA3 anomalies",
            "description": ""
        },
        {
            "id": "DOID:0060823",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060823",
            "name": "MRX94",
            "description": ""
        },
        {
            "id": "DOID:0060823",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060823",
            "name": "MRXS29",
            "description": ""
        },
        {
            "id": "DOID:0060823",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060823",
            "name": "mental retardation, X-linked 94",
            "description": ""
        },
        {
            "id": "DOID:0060823",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060823",
            "name": "syndromic X-linked mental retardation 29",
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            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060823",
            "name": "syndromic X-linked mental retardation Wu type",
            "description": ""
        },
        {
            "id": "MONDO:0010402",
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            "url": "https://monarchinitiative.org/disease/MONDO:0010402",
            "name": "syndromic X-linked intellectual disability 94",
            "description": "A syndromic X-linked intellectual disability characterized by moderate intellectual disability with variable occurrence of asthenic body habitus, dysmorphic features, autistic features, macrocephaly, seizures, myoclonic jerks, and hyporeflexia that has material basis in mutation in the GRIA3 gene on chromosome Xq25."
        },
        {
            "id": "MONDO:0010402",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010402",
            "name": "MRX94",
            "description": ""
        },
        {
            "id": "MONDO:0010402",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010402",
            "name": "MRXS29",
            "description": ""
        },
        {
            "id": "MONDO:0010402",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010402",
            "name": "intellectual developmental disorder, X-linked, syndromic, Wu type, X-linked recessive",
            "description": ""
        },
        {
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            "resource": "MONDO",
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            "description": ""
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        {
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            "name": "mental retardation, X-linked 94",
            "description": ""
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            "name": "syndromic X-linked intellectual disability 29",
            "description": ""
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            "name": "syndromic X-linked intellectual disability 94",
            "description": ""
        },
        {
            "id": "MONDO:0010402",
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            "url": "https://monarchinitiative.org/disease/MONDO:0010402",
            "name": "syndromic X-linked intellectual disability Wu type",
            "description": ""
        },
        {
            "id": "MONDO:0010402",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010402",
            "name": "syndromic X-linked intellectual disability type 94",
            "description": ""
        },
        {
            "id": "MONDO:0010402",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010402",
            "name": "MRXSW",
            "description": ""
        },
        {
            "id": "MONDO:0010402",
            "resource": "MONDO",
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            "name": "intellectual disability, X-linked, syndromic, Wu type",
            "description": ""
        },
        {
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            "name": "mental retardation, X-linked, syndromic 29",
            "description": ""
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        {
            "id": "MONDO:0010402",
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            "url": "https://monarchinitiative.org/disease/MONDO:0010402",
            "name": "mental retardation, X-linked, syndromic, Wu type",
            "description": ""
        },
        {
            "id": "MIM:300699",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/300699",
            "name": "Intellectual developmental disorder, X-linked, syndromic, Wu type",
            "description": "Intellectual developmental disorder, X-linked, syndromic, Wu type"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060823"
    ],
    "unlinked_id_list": []
}