{
    "disease_id": "DOID:0090025", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009525", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009525", 
            "name": "split hand-foot malformation type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009525", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009525", 
            "name": "split-hand/foot malformation type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009525", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009525", 
            "name": "chromosome 10Q24 Duplication syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009525", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009525", 
            "name": "10q24 microduplication syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009525", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009525", 
            "name": "Buttiens-Fryns syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009525", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009525", 
            "name": "split-hand/foot malformation 3; SHFM3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009525", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009525", 
            "name": "distal limb deficiencies with micrognathia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009525", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009525", 
            "name": "Buttiens Fryns syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009525", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009525", 
            "name": "distal limb deficiencies-micrognathia syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009525", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009525", 
            "name": "limb deficiencies, distal, with micrognathia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009525", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009525", 
            "name": "limb deficiencies distal with micrognathia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009525", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009525", 
            "name": "SHFM3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009525", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009525", 
            "name": "split-hand/foot malformation 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009525", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009525", 
            "name": "Shsf3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090025", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090025", 
            "name": "SHFM3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090025", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090025", 
            "name": "chromosome 10q24 duplication syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090025", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090025", 
            "name": "distal limb deficiencies with micrognathia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090025", 
        "description": "A split-hand/foot malformation that has_material_basis_in a contiguous gene duplication syndrome on chromosome 10q24.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090025", 
        "name": "split hand-foot malformation 3"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0090025#disease-associations", 
            "id": "0090025", 
            "database": "Alliance of Genome Resources"
        }
    ]
}