{
    "disease_id": "DOID:0090077", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012528", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012528", 
            "name": "PROK2 hypogonadotropic hypogonadism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012528", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012528", 
            "name": "hypogonadotropic hypogonadism caused by mutation in PROK2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012528", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012528", 
            "name": "Kallman syndrome 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012528", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012528", 
            "name": "hypogonadotropic hypogonadism 4 with or without anosmia; HH4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012528", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012528", 
            "name": "Kallmann syndrome 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012528", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012528", 
            "name": "KAL4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012528", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012528", 
            "name": "HH4"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090077", 
        "description": "A hypogonadotropic hypogonadism that has_material_basis_in heterozygous mutation in the prokineticin-2 gene (PROK2) on chromosome 3p13, sometimes in association with mutation in another gene.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090077", 
        "name": "hypogonadotropic hypogonadism 4 with or without anosmia"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/610628", 
            "id": "610628", 
            "database": "MIM"
        }
    ]
}