{
    "disease_id": "DOID:0111357",
    "recommended_name": {
        "id": "DOID:0111357",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111357",
        "name": "adermatoglyphia",
        "description": "A skin disease characterized by lack of epidermal ridges on the fingers, toes, palms and soles that has_material_basis_in heterozygous mutation in the SMARCAD1 gene on chromosome 4q22.3."
    },
    "synonyms": [
        {
            "id": "DOID:0111357",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111357",
            "name": "ADERM",
            "description": ""
        },
        {
            "id": "DOID:0111357",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111357",
            "name": "ADG",
            "description": ""
        },
        {
            "id": "DOID:0111357",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111357",
            "name": "Absence of fingerprints",
            "description": ""
        },
        {
            "id": "DOID:0111357",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111357",
            "name": "Congenital absence of fingerprints",
            "description": ""
        },
        {
            "id": "DOID:0111357",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111357",
            "name": "Immigration delay disease",
            "description": ""
        },
        {
            "id": "DOID:0111357",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111357",
            "name": "Isolated congenital adermatoglyphia",
            "description": ""
        },
        {
            "id": "MONDO:0007619",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007619",
            "name": "isolated congenital adermatoglyphia",
            "description": "Isolated congenital adermatoglyphia is a rare, genetic develomental defect during embryogenesis disorder characterized by the lack of epidermal ridges on the palms and soles, resulting in the absence of fingerprints, with no other associated manifestations. It is associated with a reduced number of sweat gland openings and reduced transpiration of palms and soles."
        },
        {
            "id": "MONDO:0007619",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007619",
            "name": "ADG",
            "description": ""
        },
        {
            "id": "MONDO:0007619",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007619",
            "name": "absence of fingerprints",
            "description": ""
        },
        {
            "id": "MONDO:0007619",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007619",
            "name": "adermatoglyphia",
            "description": ""
        },
        {
            "id": "MONDO:0007619",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007619",
            "name": "fingerprints, absence of",
            "description": ""
        },
        {
            "id": "MONDO:0007619",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007619",
            "name": "ADERM",
            "description": ""
        },
        {
            "id": "MONDO:0007619",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007619",
            "name": "congenital absence of fingerprints",
            "description": ""
        },
        {
            "id": "MONDO:0007619",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007619",
            "name": "immigration delay disease",
            "description": ""
        },
        {
            "id": "MONDO:0007619",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007619",
            "name": "isolated congenital adermatoglyphia",
            "description": ""
        },
        {
            "id": "MIM:136000",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/136000",
            "name": "Adermatoglyphia",
            "description": "Adermatoglyphia"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111357"
    ],
    "unlinked_id_list": []
}