{
    "disease_id": "DOID:0060234", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008710", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008710", 
            "name": "Carpenter syndrome 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008710", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008710", 
            "name": "acrocephalopolysyndactyly type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008710", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008710", 
            "name": "Carpenter syndrome type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008710", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008710", 
            "name": "Carpenter syndrome caused by mutation in RAB23"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008710", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008710", 
            "name": "CRPT1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008710", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008710", 
            "name": "RAB23 Carpenter syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008710", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008710", 
            "name": "CARPENTER syndrome 1; CRPT1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008710", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008710", 
            "name": "ACPS 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060234", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060234", 
            "name": "acrocephalopolysyndactyly type II"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060234", 
        "description": "An acrocephalosyndactylia characterized by craniosynostosis, acrocephaly, obesity, syndactyly and polydactyly.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060234", 
        "name": "Carpenter syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060234#disease-associations", 
            "id": "0060234", 
            "database": "Alliance of Genome Resources"
        }
    ]
}