{
    "disease_id": "DOID:0080627",
    "recommended_name": {
        "id": "DOID:0080627",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080627",
        "name": "alopecia-mental retardation syndrome",
        "description": "A syndrome that is characterized by loss of hair on the scalp, eyebrows, eyelashes, axillas and pubic hair, in addition to mild to severe intellectual disability."
    },
    "synonyms": [
        {
            "id": "MONDO:0021035",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0021035",
            "name": "alopecia-intellectual disability syndrome 1",
            "description": ""
        },
        {
            "id": "MONDO:0021035",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0021035",
            "name": "APMR",
            "description": ""
        },
        {
            "id": "MONDO:0021035",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0021035",
            "name": "APMR1",
            "description": ""
        },
        {
            "id": "MONDO:0021035",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0021035",
            "name": "alopecia-intellectual disability syndrome 1",
            "description": ""
        },
        {
            "id": "MONDO:0021035",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0021035",
            "name": "alopecia-mental retardation syndrome 1",
            "description": ""
        },
        {
            "id": "MIM:203650",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/203650",
            "name": "Alopecia-intellectual disability syndrome 1",
            "description": "Alopecia-intellectual disability syndrome 1"
        }
    ],
    "children": [
        {
            "id": "DOID:0080628",
            "label": "alopecia-mental retardation syndrome 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0080950",
            "label": "alopecia-mental retardation syndrome 4",
            "link_status": true,
            "children": []
        }
    ],
    "id_list": [
        "DOID:0080950",
        "DOID:0080628",
        "DOID:0080627"
    ],
    "unlinked_id_list": [],
    "crossref": [
        {
            "id": "DOID:0080627",
            "database": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0080627",
            "categories": []
        },
        {
            "id": "MONDO:0021035",
            "database": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0021035",
            "categories": []
        },
        {
            "id": "MIM:203650",
            "database": "MIM",
            "url": "https://www.omim.org/entry/203650",
            "categories": []
        }
    ],
    "proteins": [
        {
            "uniprot_canonical_ac": "P02765-1",
            "uniprot_ac": "P02765",
            "uniprot_id": "FETUA_HUMAN",
            "refseq_ac": "NP_001613",
            "glycoprotein": "yes",
            "species": [
                {
                    "name": "Homo sapiens",
                    "taxid": 9606,
                    "common_name": "Human",
                    "glygen_name": "Human",
                    "reference_species": "Homo sapiens [9606]"
                }
            ],
            "protein_names": [
                {
                    "name": "Alpha-2-HS-glycoprotein",
                    "type": "recommended"
                },
                {
                    "name": "Alpha-2-Z-globulin",
                    "type": "synonym"
                },
                {
                    "name": "Ba-alpha-2-glycoprotein",
                    "type": "synonym"
                },
                {
                    "name": "Fetuin-A",
                    "type": "synonym"
                },
                {
                    "name": "alpha-2-HS-glycoprotein isoform 2 preproprotein",
                    "type": "synonym"
                },
                {
                    "name": "alpha-2-Z-globulin",
                    "type": "synonym"
                },
                {
                    "name": "ba-alpha-2-glycoprotein",
                    "type": "synonym"
                },
                {
                    "name": "fetuin-A",
                    "type": "synonym"
                }
            ],
            "gene_names": [
                {
                    "name": "AHSG",
                    "type": "recommended"
                },
                {
                    "name": "A2HS",
                    "type": "synonym"
                },
                {
                    "name": "AHSG",
                    "type": "synonym"
                },
                {
                    "name": "AHS",
                    "type": "synonym"
                },
                {
                    "name": "APMR1",
                    "type": "synonym"
                },
                {
                    "name": "FETUA",
                    "type": "synonym"
                },
                {
                    "name": "HSGA",
                    "type": "synonym"
                },
                {
                    "name": "PRO2743",
                    "type": "synonym"
                }
            ],
            "record_id": "P02765-1",
            "evidence": [
                {
                    "id": "203650",
                    "database": "MIM",
                    "url": "https://www.omim.org/entry/203650"
                }
            ]
        }
    ],
    "glycans": [],
    "biomarkers": [],
    "association_flag": "1000",
    "record_id": "doid.0080627"
}