{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014006", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014006", 
            "name": "intellectual disability-craniofacial dysmorphism-cryptorchidism syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014006", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014006", 
            "name": "autosomal dominant intellectual disability-17"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014006", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014006", 
            "name": "MRD17"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014006", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014006", 
            "name": "PACS1-related syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014006", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014006", 
            "name": "mental retardation, autosomal dominant type 17"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014006", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014006", 
            "name": "Schuurs-Hoeijmakers syndrome; SHMS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014006", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014006", 
            "name": "autosomal dominant mental retardation 17"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014006", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014006", 
            "name": "SHMS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014006", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014006", 
            "name": "mental retardation, autosomal dominant 17"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014006", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014006", 
            "name": "mental retardation, autosomal dominant 17; MRD17"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070047", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070047", 
            "name": "MRD17"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070047", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070047", 
            "name": "SHMS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070047", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070047", 
            "name": "autosomal dominant mental retardation 17"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070047", 
        "description": "An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of PACS1 on chromosome 11q13.1-q13.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070047", 
        "name": "Schuurs-Hoeijmakers Syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/615009", 
            "id": "615009", 
            "database": "MIM"
        }
    ]
}