{
    "disease_id": "DOID:0080082",
    "recommended_name": {
        "id": "DOID:0080082",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080082",
        "name": "nonsyndromic congenital nail disorder 4",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0080082",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0080082",
            "name": "HYPONYCHIA CONGENITA",
            "description": ""
        },
        {
            "id": "DOID:0080082",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0080082",
            "name": "anonychia congenita",
            "description": ""
        },
        {
            "id": "MONDO:0008798",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008798",
            "name": "nonsyndromic congenital nail disorder 4",
            "description": "Any isolated congenital anonychia in which the cause of the disease is a mutation in the RSPO4 gene."
        },
        {
            "id": "MONDO:0008798",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008798",
            "name": "RSPO4 isolated congenital anonychia",
            "description": ""
        },
        {
            "id": "MONDO:0008798",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008798",
            "name": "isolated congenital anonychia caused by mutation in RSPO4",
            "description": ""
        },
        {
            "id": "MONDO:0008798",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008798",
            "name": "nail disorder, nonsyndromic congenital, type 4",
            "description": ""
        },
        {
            "id": "MONDO:0008798",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008798",
            "name": "nonsyndromic congenital nail disorder 4",
            "description": ""
        },
        {
            "id": "MONDO:0008798",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008798",
            "name": "nonsyndromic congenital nail disorder type 4",
            "description": ""
        },
        {
            "id": "MONDO:0008798",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008798",
            "name": "NDNC4",
            "description": ""
        },
        {
            "id": "MONDO:0008798",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008798",
            "name": "nail disorder, nonsyndromic congenital, 4",
            "description": ""
        },
        {
            "id": "MIM:206800",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/206800",
            "name": "Nail disorder, non-syndromic congenital, 4",
            "description": "Nail disorder, non-syndromic congenital, 4"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080082"
    ],
    "unlinked_id_list": []
}