{
    "disease_id": "DOID:0090085", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013911", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013911", 
            "name": "hypogonadotropic hypogonadism caused by mutation in NSMF"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013911", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013911", 
            "name": "hypogonadotropic hypogonadism 9 with or without anosmia; HH9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013911", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013911", 
            "name": "HH9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013911", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013911", 
            "name": "NSMF hypogonadotropic hypogonadism"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090085", 
        "description": "A hypogonadotropic hypogonadism that is characterized by autosomal dominant inheritance and has_material_basis_in heterozygous mutation in the NELF gene on chromosome 9q34, sometimes in association with mutation in another gene.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090085", 
        "name": "hypogonadotropic hypogonadism 9 with or without anosmia"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/614838", 
            "id": "614838", 
            "database": "MIM"
        }
    ]
}