{
    "disease_id": "DOID:0080724", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007478", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007478", 
            "name": "autosomal dominant Kenny-Caffey syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007478", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007478", 
            "name": "dwarfism, cortical thickening of tubular bones and transient hypocalcemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007478", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007478", 
            "name": "Kenny-Caffey syndrome, type 2; KCS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007478", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007478", 
            "name": "Kenny syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007478", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007478", 
            "name": "Kenny-Caffey syndrome, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007478", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007478", 
            "name": "Kenny-Caffey syndrome, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007478", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007478", 
            "name": "Kenny-Caffey syndrome type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007478", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007478", 
            "name": "dwarfism, cortical thickening of tubular bones, and transient hypocalcemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007478", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007478", 
            "name": "KCS2"
        }, 
        {
            "url": "https://www.omim.org/entry/127000", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:127000", 
            "name": "Kenny-Caffey syndrome 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080724", 
        "description": "A syndrome that is characterized by growth retardation with proportionate short stature, cortical thickening and medullary stenosis of the long bones, delayed anterior fontanelle closure, hypocalcemia due to congenital hypoparathyroidism and facial dysmorphism, including prominent forehead, microphthalmia, and micrognathia.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080724", 
        "name": "Kenny-Caffey syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/127000", 
            "id": "127000", 
            "database": "MIM"
        }
    ]
}