{
    "disease_id": "DOID:0111627", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009079", 
            "description": "", 
            "resource": "MONDO", 
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            "name": "autosomal recessive deafness-onychodystrophy syndrome"
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009079", 
            "name": "door syndrome"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009079", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009079", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009079", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009079", 
            "description": "", 
            "resource": "MONDO", 
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            "name": "DOORS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009079", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009079", 
            "name": "brachydactyly due to absence of distal phalanges"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009079", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009079", 
            "name": "deafness onychodystrophy osteodystrophy and mental retardation syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009079", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009079", 
            "name": "deafness-onychoosteodystrophy-intellectual disability syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009079", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009079", 
            "name": "Eronen syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009079", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009079", 
            "name": "drc syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009079", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009079", 
            "name": "deafness, onychodystrophy, osteodystrophy, mental retardation, and seizures syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009079", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009079", 
            "name": "deafness-onychodystrophy-osteodystrophy-intellectual disability-seizures syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009079", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009079", 
            "name": "Digitorenocerebral syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111627", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111627", 
            "name": "deafness-onychodystrophy-osteodystrophy-intellectual disability-seizures syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111627", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111627", 
            "name": "deafness-onychodystrophy-osteodystrophy-intellectual disability syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111627", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111627", 
            "name": "DOOR syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111627", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111627", 
            "name": "DOORS"
        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111627", 
            "name": "deafness-onychoosteodystrophy-intellectual disability syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111627", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111627", 
            "name": "autosomal recessive deafness-onychodystrophy syndrome"
        }, 
        {
            "url": "https://www.omim.org/entry/220500", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:220500", 
            "name": "Deafness, onychodystrophy, osteodystrophy, mental retardation, and seizures syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111627", 
        "description": "A syndrome characterized by sensorineural deafness, onychodystrophy, osteodystrophy, seizures, and intellectual disability that has_material_basis_in homozygous or compound heterozygous mutation in TBC1D24 on chromosome 16p13.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111627", 
        "name": "DOORS syndrome"
    }, 
    "evidence": [
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            "url": "https://www.omim.org/entry/220500", 
            "id": "220500", 
            "database": "MIM"
        }
    ]
}