{
    "disease_id": "DOID:0090070", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007844", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007844", 
            "name": "hypogonadotropic hypogonadism 2 with or without anosmia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007844", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007844", 
            "name": "KAL2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007844", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007844", 
            "name": "HH2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007844", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007844", 
            "name": "Kallmann syndrome 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007844", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007844", 
            "name": "hypogonadotropic hypogonadism 2 with or without anosmia; HH2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007844", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007844", 
            "name": "FGFR1 hypogonadotropic hypogonadism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007844", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007844", 
            "name": "hypogonadotropic hypogonadism caused by mutation in FGFR1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090070", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090070", 
            "name": "hypogonadotropism"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090070", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090070", 
            "name": "congenital idiopathic hypogonadotropic hypogonadism"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090070", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090070", 
            "name": "isolated congenital gonadotropin deficiency"
        }, 
        {
            "url": "https://www.omim.org/entry/147950", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:147950", 
            "name": "Hypogonadotropic hypogonadism 2 with or without anosmia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090070", 
        "description": "A hypogonadism characterized by a impaired signalling by gonadotrpin relasing hormone.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090070", 
        "name": "hypogonadotropic hypogonadism"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/147950", 
            "id": "147950", 
            "database": "MIM"
        }
    ]
}