{
    "disease_id": "DOID:0060485", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009341", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009341", 
            "name": "microcephaly, mental retardation, and distinct facial featrues, with or without Hirschprung disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009341", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009341", 
            "name": "Hirschsprung disease mental retardation syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009341", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009341", 
            "name": "mental retardation, microcephaly, and distinct facial features with or without Hirschsprung disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009341", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009341", 
            "name": "MOWS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009341", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009341", 
            "name": "Mowat-Wilson syndrome; MOWS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009341", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009341", 
            "name": "microcephaly, mental retardation, and distinct Facial features, with or without Hirschsprung disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009341", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009341", 
            "name": "Hirschsprung disease-mental retardation syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009341", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009341", 
            "name": "Hirschsprung disease-intellectual disability syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060485", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060485", 
            "name": "Hirschsprung disease mental retardation syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060485", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060485", 
            "name": "microcephaly, mental retardation, and distinct facial featrues, with or without Hirschprung disease"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060485", 
        "description": "A syndrome characterized by distinctive facial features, intellectual disability, delayed development, Hirschsprung disease and has_material_basis_in de novo heterozygous mutation in the ZEB2 gene on chromosome 2q22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060485", 
        "name": "Mowat-Wilson syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060485#disease-associations", 
            "id": "0060485", 
            "database": "Alliance of Genome Resources"
        }
    ]
}