{
    "disease_id": "DOID:0090024", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009080", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009080", 
            "name": "split-hand/foot malformation 1 with sensorineural hearing loss, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009080", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009080", 
            "name": "deafness, congenital, with split hands and feet"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009080", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009080", 
            "name": "congenital deafness with split hands and feet"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009080", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009080", 
            "name": "split-hand/foot malformation 1 with sensorineural hearing loss, autosomal recessive; SHFM1D"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009080", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009080", 
            "name": "SHFM1D"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009080", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009080", 
            "name": "split hand-split foot-deafness syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090024", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090024", 
            "name": "SHFM1D"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090024", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090024", 
            "name": "congenital deafness with split hands and feet"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090024", 
        "description": "A split-hand/foot malformation characterized by split-hand/foot malformation and sensorineural hearing impairment that has_material_basis_in homozygous mutation in the DLX5 gene on chromosome 7q21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090024", 
        "name": "split hand-foot malformation 1 with sensorineural hearing loss"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0090024#disease-associations", 
            "id": "0090024", 
            "database": "Alliance of Genome Resources"
        }
    ]
}