{
    "disease_id": "DOID:0110710", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014390", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014390", 
            "name": "hypotrichosis caused by mutation in KRT71"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014390", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014390", 
            "name": "HYPT13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014390", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014390", 
            "name": "hypotrichosis 13; HYPT13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014390", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014390", 
            "name": "hypotrichosis type 13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014390", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014390", 
            "name": "hypotrichosis with woolly hair"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014390", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014390", 
            "name": "KRT71 hypotrichosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110710", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110710", 
            "name": "Hypt13"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110710", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110710", 
            "name": "hypotrichosis with woolly hair"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110710", 
        "description": "A hypotrichosis that has_material_basis_in a autosomal dominant mutation of KRT71 on chromosome 12q13.13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110710", 
        "name": "hypotrichosis 13"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110710#disease-associations", 
            "id": "0110710", 
            "database": "Alliance of Genome Resources"
        }
    ]
}