{
    "disease_id": "DOID:0090026", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009157", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009157", 
            "name": "split hand-foot malformation caused by mutation in WNT10B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009157", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009157", 
            "name": "WNT10B split hand-foot malformation"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009157", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009157", 
            "name": "split-hand/foot malformation 6; SHFM6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009157", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009157", 
            "name": "split hand-foot malformation type 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009157", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009157", 
            "name": "SHFM6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009157", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009157", 
            "name": "split-hand/foot malformation 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009157", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009157", 
            "name": "split-hand/foot malformation type 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009157", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009157", 
            "name": "ectrodactyly, autosomal recessive"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090026", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090026", 
            "name": "SHFM6"
        }, 
        {
            "url": "https://www.omim.org/entry/225300", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:225300", 
            "name": "Split-hand/foot malformation 6"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090026", 
        "description": "A split-hand/foot malformation that has_material_basis_in homozygous mutation in the WNT10B gene on chromosome 12q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090026", 
        "name": "split hand-foot malformation 6"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/225300", 
            "id": "225300", 
            "database": "MIM"
        }
    ]
}