{
    "disease_id": "DOID:0111574", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014765", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014765", 
            "name": "woolly hair, autosomal recessive 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014765", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014765", 
            "name": "woolly hair, autosomal recessive type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014765", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014765", 
            "name": "woolly hair, autosomal recessive 3, with hypotrichosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014765", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014765", 
            "name": "KRT25 woolly hair (disease)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014765", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014765", 
            "name": "ARWH3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014765", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014765", 
            "name": "woolly hair (disease) caused by mutation in KRT25"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014765", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014765", 
            "name": "woolly hair, autosomal recessive 3; ARWH3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111574", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111574", 
            "name": "ARWH3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111574", 
        "description": "A familial woolly hair syndrome that has_material_basis_in homozygous or compound heterozygous mutation in KRT24 on chromosome 17q21.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111574", 
        "name": "autosomal recessive woolly hair 3"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111574#disease-associations", 
            "id": "0111574", 
            "database": "Alliance of Genome Resources"
        }
    ]
}