{
    "disease_id": "DOID:0111647",
    "recommended_name": {
        "id": "DOID:0111647",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111647",
        "name": "Schopf-Schulz-Passarge syndrome",
        "description": "An ectodermal dysplasia characterized by multiple eyelid apocrine hidrocystomas, palmoplantar keratoderma, hypotrichosis, hypodontia and nail dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the WNT10A gene on chromosome 2q35."
    },
    "synonyms": [
        {
            "id": "DOID:0111647",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111647",
            "name": "SSPS",
            "description": ""
        },
        {
            "id": "DOID:0111647",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111647",
            "name": "eccrine tumors-ectodermal dysplasia",
            "description": ""
        },
        {
            "id": "DOID:0111647",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111647",
            "name": "keratosis palmoplantaris-cystic eyelids-hypodontia-hypotrichosis syndrome",
            "description": ""
        },
        {
            "id": "DOID:0111647",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111647",
            "name": "palmoplantar keratoderma-cystic eyelids-hypodontia-hypotrichosis syndrome",
            "description": ""
        },
        {
            "id": "DOID:0111647",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111647",
            "name": "palmoplantar hyperkeratosis-cystic eyelids-hypodontia-hypotrichosis syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009145",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009145",
            "name": "Schpf-Schulz-Passarge syndrome",
            "description": "A rare autosomal recessive ectodermal dysplasia characterized by multiple eyelid apocrine hidrocystomas, palmoplantar keratoderma, hypotrichosis, hypodontia and nail dystrophy."
        },
        {
            "id": "MONDO:0009145",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009145",
            "name": "SSPS",
            "description": ""
        },
        {
            "id": "MONDO:0009145",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009145",
            "name": "eccrine tumors-ectodermal dysplasia",
            "description": ""
        },
        {
            "id": "MONDO:0009145",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009145",
            "name": "keratosis palmoplantaris-cystic eyelids-hypodontia-hypotrichosis syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009145",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009145",
            "name": "palmoplantar hyperkeratosis-cystic eyelids-hypodontia-hypotrichosis syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009145",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009145",
            "name": "palmoplantar keratoderma-cystic eyelids-hypodontia-hypotrichosis syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009145",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009145",
            "name": "SCHOPF-Schulz-Passarge syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009145",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009145",
            "name": "eccrine tumours with ectodermal dysplasia",
            "description": ""
        },
        {
            "id": "MIM:224750",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/224750",
            "name": "Schopf-Schulz-Passarge syndrome",
            "description": "Schopf-Schulz-Passarge syndrome"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111647"
    ],
    "unlinked_id_list": []
}