{
    "disease_id": "DOID:0111545", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008303", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008303", 
            "name": "precocious puberty, male-limited"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008303", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008303", 
            "name": "peripheral precocious puberty caused by mutation in LHCGR"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008303", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008303", 
            "name": "sexual precocity, familial, gonadotropin-independent"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008303", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008303", 
            "name": "familial gonadotropin-independent male-limited sexual precocity"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008303", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008303", 
            "name": "testotoxicosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008303", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008303", 
            "name": "testotoxicosis, familial"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008303", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008303", 
            "name": "precocious puberty, male limited"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008303", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008303", 
            "name": "male-limited precocious puberty"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008303", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008303", 
            "name": "LHCGR peripheral precocious puberty"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008303", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008303", 
            "name": "familial Testotoxicosis (subtype)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008303", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008303", 
            "name": "Leydig cell adenoma, somatic, with male-limited precocious puberty"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008303", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008303", 
            "name": "FMPP"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008303", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008303", 
            "name": "pubertas praecox"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111545", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111545", 
            "name": "FMPP"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111545", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111545", 
            "name": "male-limited precocious puberty"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111545", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111545", 
            "name": "testotoxicosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111545", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111545", 
            "name": "familial gonadotropin-independent male-limited sexual precocity"
        }, 
        {
            "url": "https://www.omim.org/entry/176410", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:176410", 
            "name": "Familial male precocious puberty"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111545", 
        "description": "An endocrine system disease characterized by onset in early childhood of accelerated growth, early development of secondary sexual characteristics, and reduced adult height in males only that has_material_basis_in heterozygous mutation in LHCGR on chromosome 2p16.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111545", 
        "name": "familial male-limited precocious puberty"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/176410", 
            "id": "176410", 
            "database": "MIM"
        }
    ]
}