{
    "disease_id": "DOID:0050601",
    "recommended_name": {
        "id": "DOID:0050601",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0050601",
        "name": "ADULT syndrome",
        "description": "A syndrome that is characterized by light pigmentation with excessive freckling, sparse hair involving the scalp and axilla, lacrimal duct stenosis or atresia, onychodysplasia, hypodontia or early loss of permanent teeth, athelia or hypoplastic nipples, and breast hypoplasia, has_material_basis_in heterozygous mutation in the TP63 gene on chromosome 3q28."
    },
    "synonyms": [
        {
            "id": "DOID:0050601",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050601",
            "name": "acro-dermato-ungual-lacrimal-tooth syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007072",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007072",
            "name": "ADULT syndrome",
            "description": "ADULT (Acro-dermo-ungual-lacrimal-tooth) syndrome is a rare ectodermal dysplasia syndrome characterized by ectrodactyly, syndactyly, mammary hypoplasia, and excessive freckling as well as other typical ectodermal defects such as hypodontia, lacrimal duct anomalies, hypotrichosis, and onychodysplasia."
        },
        {
            "id": "MONDO:0007072",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007072",
            "name": "ADULT syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007072",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007072",
            "name": "acro-dermato-ungual-lacrimal-tooth syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007072",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007072",
            "name": "acrodermatounguallacrimaltooth syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007072",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007072",
            "name": "pigment anomaly-ectrodactyly-hypodontia syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007072",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007072",
            "name": "acro dermato ungual lacrimal tooth syndrome",
            "description": ""
        },
        {
            "id": "MIM:103285",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/103285",
            "name": "Acro-dermato-ungual-lacrimal-tooth syndrome",
            "description": "Acro-dermato-ungual-lacrimal-tooth syndrome"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0050601"
    ],
    "unlinked_id_list": []
}