{
    "disease_id": "DOID:0110704", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011452", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011452", 
            "name": "hypotrichosis, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011452", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011452", 
            "name": "total Mari type hypotrichosis,"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011452", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011452", 
            "name": "Wh/Ht"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011452", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011452", 
            "name": "hypotrichosis, localized, autosomal recessive 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011452", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011452", 
            "name": "hypotrichosis, total, Mari type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011452", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011452", 
            "name": "hypotrichosis 7; HYPT7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011452", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011452", 
            "name": "HYPT7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011452", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011452", 
            "name": "Mari type alopecia universalis congenita"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011452", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011452", 
            "name": "hypotrichosis caused by mutation in LIPH"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011452", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011452", 
            "name": "LIPH hypotrichosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011452", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011452", 
            "name": "alopecia universalis congenita, Mari type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011452", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011452", 
            "name": "hypotrichosis type 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011452", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011452", 
            "name": "woolly hair, autosomal recessive 2, with or without hypotrichosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011452", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011452", 
            "name": "total hypotrichosis, Mari type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011452", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011452", 
            "name": "Lah2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110704", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110704", 
            "name": "Hypt7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110704", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110704", 
            "name": "Lah2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110704", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110704", 
            "name": "hypotrichosis, localized, autosomal recessive 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110704", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110704", 
            "name": "total Mari type hypotrichosis,"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110704", 
        "description": "A hypotrichosis that has_material_basis_in a autosomal recessive mutation of LIPH on chromosome 3q27.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110704", 
        "name": "hypotrichosis 7"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110704#disease-associations", 
            "id": "0110704", 
            "database": "Alliance of Genome Resources"
        }
    ]
}