{
    "disease_id": "DOID:0080082", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008798", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008798", 
            "name": "HYPONYCHIA congenita"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008798", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008798", 
            "name": "nail disorder, nonsyndromic congenital, 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008798", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008798", 
            "name": "anonychia/hyponychia congenita"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008798", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008798", 
            "name": "anonychia congenita"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008798", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008798", 
            "name": "NDNC4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008798", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008798", 
            "name": "RSPO4 isolated congenital anonychia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008798", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008798", 
            "name": "nail disorder, nonsyndromic congenital, type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008798", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008798", 
            "name": "isolated congenital anonychia caused by mutation in RSPO4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008798", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008798", 
            "name": "nonsyndromic congenital nail disorder type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008798", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008798", 
            "name": "anonychia congenita totalis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008798", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008798", 
            "name": "nail disorder, nonsyndromic congenital, 4; NDNC4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008798", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008798", 
            "name": "anonychia totalis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080082", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080082", 
            "name": "HYPONYCHIA CONGENITA"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080082", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080082", 
            "name": "anonychia congenita"
        }, 
        {
            "url": "https://www.omim.org/entry/206800", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:206800", 
            "name": "Nail disorder, non-syndromic congenital, 4"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080082", 
        "description": "A nonsyndromic congenital nail disorder that is characterized by complete absence or severe hypoplasia of all fingernails and toenails without significant bone anomalies, and that has_material_basis_in homozygous or compound heterozygous mutation in the R-spondin-4 gene on chromosome 20p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080082", 
        "name": "nonsyndromic congenital nail disorder 4"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/206800", 
            "id": "206800", 
            "database": "MIM"
        }
    ]
}