{
    "disease_id": "DOID:0110090", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013569", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013569", 
            "name": "SRTD7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013569", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013569", 
            "name": "short rib-polydactyly syndrom type V"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013569", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013569", 
            "name": "short-rib thoracic dysplasia 7 with or without polydactyly; SRTD7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013569", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013569", 
            "name": "short rib-polydactyly syndrome, type 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013569", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013569", 
            "name": "SRPS5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110090", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110090", 
            "name": "SRPS5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110090", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110090", 
            "name": "SRTD7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110090", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110090", 
            "name": "short rib-polydactyly syndrome type V"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110090", 
        "description": "An asphyxiating thoracic dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the WDR35 gene on chromosome 2p21.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110090", 
        "name": "short-rib thoracic dysplasia 7 with or without polydactyly"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/614091", 
            "id": "614091", 
            "database": "MIM"
        }
    ]
}