{
    "disease_id": "DOID:0112043",
    "recommended_name": {
        "id": "DOID:0112043",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0112043",
        "name": "non-syndromic X-linked intellectual disability 91",
        "description": "A non-syndromic X-linked intellectual disability characterized by severe intellectual disability that has_material_basis_in heterozygous mutation in a region on chromosome Xq13.3."
    },
    "synonyms": [
        {
            "id": "DOID:0112043",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112043",
            "name": "MRX91",
            "description": ""
        },
        {
            "id": "DOID:0112043",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112043",
            "name": "X-linked mental retardation 91",
            "description": ""
        },
        {
            "id": "MONDO:0010363",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010363",
            "name": "intellectual disability, X-linked 91",
            "description": ""
        },
        {
            "id": "MONDO:0010363",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010363",
            "name": "intellectual disability, X-linked 91",
            "description": ""
        },
        {
            "id": "MONDO:0010363",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010363",
            "name": "intellectual disability, X-linked type 91",
            "description": ""
        },
        {
            "id": "MONDO:0010363",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010363",
            "name": "mental retardation, X-linked 91, X-linked dominant",
            "description": ""
        },
        {
            "id": "MONDO:0010363",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010363",
            "name": "mental retardation, X-linked type 91",
            "description": ""
        },
        {
            "id": "MONDO:0010363",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010363",
            "name": "MRX91",
            "description": ""
        },
        {
            "id": "MONDO:0010363",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010363",
            "name": "mental retardation, X-linked 91",
            "description": ""
        },
        {
            "id": "MIM:300577",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/300577",
            "name": "Intellectual developmental disorder, X-linked 91",
            "description": "Intellectual developmental disorder, X-linked 91"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0112043"
    ],
    "unlinked_id_list": [],
    "crossref": [
        {
            "id": "DOID:0112043",
            "database": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112043",
            "categories": []
        },
        {
            "id": "MONDO:0010363",
            "database": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010363",
            "categories": []
        },
        {
            "id": "MIM:300577",
            "database": "MIM",
            "url": "https://www.omim.org/entry/300577",
            "categories": []
        }
    ],
    "proteins": [
        {
            "uniprot_canonical_ac": "Q96MV8-1",
            "uniprot_ac": "Q96MV8",
            "uniprot_id": "ZDH15_HUMAN",
            "refseq_ac": "NP_001139728",
            "glycoprotein": "yes",
            "species": [
                {
                    "name": "Homo sapiens",
                    "taxid": 9606,
                    "common_name": "Human",
                    "glygen_name": "Human",
                    "reference_species": "Homo sapiens [9606]"
                }
            ],
            "protein_names": [
                {
                    "name": "Palmitoyltransferase ZDHHC15",
                    "type": "recommended"
                },
                {
                    "name": "2.3.1.-",
                    "type": "synonym"
                },
                {
                    "name": "2.3.1.225",
                    "type": "synonym"
                },
                {
                    "name": "Acyltransferase ZDHHC15",
                    "type": "synonym"
                },
                {
                    "name": "DHHC-15",
                    "type": "synonym"
                },
                {
                    "name": "Zinc finger DHHC domain-containing protein 15",
                    "type": "synonym"
                },
                {
                    "name": "acyltransferase ZDHHC15",
                    "type": "synonym"
                },
                {
                    "name": "palmitoyltransferase ZDHHC15 isoform 2",
                    "type": "synonym"
                },
                {
                    "name": "palmitoyltransferase ZDHHC15",
                    "type": "synonym"
                },
                {
                    "name": "zinc finger DHHC domain-containing protein 15",
                    "type": "synonym"
                },
                {
                    "name": "zinc finger DHHC-type containing 15",
                    "type": "synonym"
                },
                {
                    "name": "zinc finger DHHC-type palmitoyltransferase 15",
                    "type": "synonym"
                },
                {
                    "name": "zinc finger, DHHC domain containing 15",
                    "type": "synonym"
                }
            ],
            "gene_names": [
                {
                    "name": "ZDHHC15",
                    "type": "recommended"
                },
                {
                    "name": "DHHC15",
                    "type": "synonym"
                },
                {
                    "name": "MRX91",
                    "type": "synonym"
                },
                {
                    "name": "PRO4501",
                    "type": "synonym"
                },
                {
                    "name": "ZDHHC15",
                    "type": "synonym"
                }
            ],
            "record_id": "Q96MV8-1",
            "evidence": [
                {
                    "id": "300577",
                    "database": "MIM",
                    "url": "https://www.omim.org/entry/300577"
                }
            ]
        }
    ],
    "glycans": [],
    "biomarkers": [],
    "association_flag": "1000",
    "record_id": "doid.0112043"
}