{
    "disease_id": "DOID:1925", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007617", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007617", 
            "name": "Coffin-Siris syndrome 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007617", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007617", 
            "name": "CSS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007617", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007617", 
            "name": "fifth digit syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007617", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007617", 
            "name": "COFFIN-SIRIS syndrome 1; CSS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007617", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007617", 
            "name": "COFFIN-SIRIS syndrome; CSS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1925", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1925", 
            "name": "Dwarfism-Onychodysplasia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1925", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1925", 
            "name": "Fifth Digit Syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1925", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1925", 
            "name": "Short Stature-Onychodysplasia."
        }, 
        {
            "url": "https://www.omim.org/entry/135900", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:135900", 
            "name": "Coffin-Siris syndrome 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:1925", 
        "description": "An autosomal dominant non-syndromic intellectual disability that is characterized by mental retardation associated with coarse facial features, hypertrichosis, sparse scalp hair, and hypoplastic or absent fifth fingernails or toenails.", 
        "resource": "Disease Ontology", 
        "id": "DOID:1925", 
        "name": "Coffin-Siris syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/135900", 
            "id": "135900", 
            "database": "MIM"
        }
    ]
}