{
    "disease_id": "DOID:0090088", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009239", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009239", 
            "name": "follicle-stimulating hormone deficiency, isolated"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009239", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009239", 
            "name": "hypogonadotropic hypogonadism caused by mutation in FSHB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009239", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009239", 
            "name": "isolated follicle stimulating hormone deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009239", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009239", 
            "name": "HH24"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009239", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009239", 
            "name": "hypogonadotropic hypogonadism 24 without anosmia; HH24"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009239", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009239", 
            "name": "FSHB hypogonadotropic hypogonadism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009239", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009239", 
            "name": "isolated FSH deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009239", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009239", 
            "name": "isolated follicle-stimulating hormone (FSH) deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009239", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009239", 
            "name": "isolated follicle-stimulating hormone deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090088", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090088", 
            "name": "isolated follicle-stimulating hormone deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090088", 
        "description": "A hypogonadotropic hypogonadism that has_material_basis_in homozygous or compound heterozygous mutation in the FSHB gene on chromosome 11p14.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090088", 
        "name": "hypogonadotropic hypogonadism 24 without anosmia"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/229070", 
            "id": "229070", 
            "database": "MIM"
        }
    ]
}