{
    "disease_id": "DOID:0111647", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009145", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009145", 
            "name": "SchC6pf-Schulz-Passarge syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009145", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009145", 
            "name": "keratosis palmoplantaris-cystic eyelids-hypodontia-hypotrichosis syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009145", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009145", 
            "name": "palmoplantar keratoderma-cystic eyelids-hypodontia-hypotrichosis syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009145", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009145", 
            "name": "SChPF-Schulz-Passarge syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009145", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009145", 
            "name": "eccrine tumors-ectodermal dysplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009145", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009145", 
            "name": "eccrine tumors with ectodermal dysplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009145", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009145", 
            "name": "SSPS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009145", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009145", 
            "name": "keratosis palmoplantaris with cystic eyelids, hypodontia, and hypotrichosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009145", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009145", 
            "name": "SCHOPF-Schulz-Passarge syndrome; SSPS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009145", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009145", 
            "name": "palmoplantar hyperkeratosis-cystic eyelids-hypodontia-hypotrichosis syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111647", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111647", 
            "name": "SSPS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111647", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111647", 
            "name": "eccrine tumors-ectodermal dysplasia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111647", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111647", 
            "name": "keratosis palmoplantaris-cystic eyelids-hypodontia-hypotrichosis syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111647", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111647", 
            "name": "palmoplantar keratoderma-cystic eyelids-hypodontia-hypotrichosis syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111647", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111647", 
            "name": "palmoplantar hyperkeratosis-cystic eyelids-hypodontia-hypotrichosis syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111647", 
        "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 WNT10A on chromosome 2q35.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111647", 
        "name": "Schopf-Schulz-Passarge syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111647#disease-associations", 
            "id": "0111647", 
            "database": "Alliance of Genome Resources"
        }
    ]
}