Hypergonadotropic hypogonadism

Symptom Information:

Symptom ID: HPO:0000815
Synonyms:
Hypergonadotrophic hypogonadism [HPO:0000815]
Primary hypogonadism [HPO:0000815]
Hypergonadotrophic hypogonadism [OMIM:Hypergonadotrophic hypogonadism]
Hypergonadotropic hypogonadism [OMIM:Hypergonadotropic hypogonadism]
Primary hypogonadism [OMIM:Primary hypogonadism]
Hypergonadotrophic hypogonadism (in females in adolescence) [OMIM:Hypergonadotrophic hypogonadism (in females in adolescence)]
Hypergonadotropic hypogonadism (HCS) [OMIM:Hypergonadotropic hypogonadism (HCS)]
Hypergonadotropic hypogonadism (in a subset of patients) [OMIM:Hypergonadotropic hypogonadism (in a subset of patients)]
Hypergonadotropic hypogonadism (males) [OMIM:Hypergonadotropic hypogonadism (males)]
Hypergonadotropic hypogonadism (reported in 1 female) [OMIM:Hypergonadotropic hypogonadism (reported in 1 female)]
Hypogonadism, primary [OMIM:Hypogonadism, primary]
Primary hypogonadism (in 2 male patients) [OMIM:Primary hypogonadism (in 2 male patients)]
Primary hypogonadism [MedDRA:10052649]
Quality:
Cross references:
OMIM: "Hypergonadotrophic hypogonadism" [OMIM:Hypergonadotrophic hypogonadism]
OMIM: "Hypergonadotropic hypogonadism" [OMIM:Hypergonadotropic hypogonadism]
OMIM: "Primary hypogonadism" [OMIM:Primary hypogonadism]
OMIM: "Hypergonadotrophic hypogonadism (in females in adolescence)" [OMIM:Hypergonadotrophic hypogonadism (in females in adolescence)]
OMIM: "Hypergonadotropic hypogonadism (HCS)" [OMIM:Hypergonadotropic hypogonadism (HCS)]
OMIM: "Hypergonadotropic hypogonadism (in a subset of patients)" [OMIM:Hypergonadotropic hypogonadism (in a subset of patients)]
OMIM: "Hypergonadotropic hypogonadism (males)" [OMIM:Hypergonadotropic hypogonadism (males)]
OMIM: "Hypergonadotropic hypogonadism (reported in 1 female)" [OMIM:Hypergonadotropic hypogonadism (reported in 1 female)]
OMIM: "Hypogonadism, primary" [OMIM:Hypogonadism, primary]
OMIM: "Primary hypogonadism (in 2 male patients)" [OMIM:Primary hypogonadism (in 2 male patients)]
Is a (Direct Parents):
HPO         Hypogonadism
MedDRA Endocrine abnormalities of gonadal function NEC
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the endocrine system(HPO:0000818)
          Puberty and gonadal disorders(HPO:0008373)
             Hypogonadism(HPO:0000135)
                Hypergonadotropic hypogonadism(HPO:0000815)
       Abnormality of the genitourinary system(HPO:0000119)
          Abnormality of the genital system(HPO:0000078)
             Abnormality of reproductive system physiology(HPO:0000080)
                Hypogonadism(HPO:0000135)
                   Hypergonadotropic hypogonadism(HPO:0000815)
MedDRA:
Endocrine disorders(MedDRA:10014698)
    Endocrine disorders of gonadal function(MedDRA:10014701)
       Endocrine abnormalities of gonadal function NEC(MedDRA:10014691)
          Hypergonadotropic hypogonadism(HPO:0000815)
Database Frequency: 48 / 7739
Resource:

All diseases associated with this symptom:

2p21 microdeletion syndrome (Orphanet:163693)
46,XY complete gonadal dysgenesis (Orphanet:242)
ALPHA-METHYLACYL-CoA RACEMASE DEFICIENCY (OMIM:614307)
Alopecia - intellectual deficit - hypergonadotropic hypogonadism (Orphanet:1014)
Alström syndrome (Orphanet:64)
Aromatase deficiency (Orphanet:91)
Atypical hypotonia - cystinuria syndrome (Orphanet:238523)
Autosomal dominant progressive external ophthalmoplegia (Orphanet:254892)
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency (Orphanet:331176)
CHONDRODYSPLASIA, ACROMESOMELIC, WITH GENITAL ANOMALIES (OMIM:609441)
Classic galactosemia (Orphanet:79239)
Congenital cataracts - facial dysmorphism - neuropathy (Orphanet:48431)
Congenital lactic acidosis, Saguenay-Lac-St. Jean type (Orphanet:70472)
Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome (Orphanet:2229)
FANCONI ANEMIA, COMPLEMENTATION GROUP A (OMIM:227650)
FANCONI ANEMIA, COMPLEMENTATION GROUP C (OMIM:227645)
FANCONI ANEMIA, COMPLEMENTATION GROUP D2 (OMIM:227646)
FANCONI ANEMIA, COMPLEMENTATION GROUP E (OMIM:600901)
Faisalabad histiocytosis (Orphanet:254707)
Fanconi anemia (Orphanet:84)
H syndrome (Orphanet:168569)
Hypotonia - cystinuria syndrome (Orphanet:163690)
Infantile onset spinocerebellar ataxia (Orphanet:1186)
Intellectual deficit - dysmorphism - hypogonadism - diabetes mellitus (Orphanet:3044)
Leukoencephalopathy - dystonia - motor neuropathy (Orphanet:163684)
Leydig cell hypoplasia (Orphanet:755)
Leydig cell hypoplasia due to complete LH resistance (Orphanet:96265)
Leydig cell hypoplasia due to partial LH resistance (Orphanet:96266)
MACS syndrome (Orphanet:217335)
Male hypergonadotropic hypogonadism - intellectual deficit - skeletal anomalies (Orphanet:2234)
Marinesco-Sjögren syndrome (Orphanet:559)
Moyamoya disease - short stature - facial dysmorphism - hypergonadotropic hypogonadism (Orphanet:280679)
OVARIAN DYSGENESIS 2 (OMIM:300510)
Obesity due to leptin receptor gene deficiency (Orphanet:179494)
PMM2-CDG (Orphanet:79318)
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 1 (OMIM:157640)
Perrault Syndrome 1 (OMIM:233400)
Perrault Syndrome 3 (OMIM:614129)
Perrault Syndrome 5 (OMIM:616138)
Pigmented hypertrichosis with insulin dependent diabetes mellitus syndrome (Orphanet:254723)
Primary hypergonadotropic hypogonadism - partial alopecia (Orphanet:2232)
Progressive external ophthalmoplegia - myopathy - emaciation (Orphanet:352447)
Retinitis pigmentosa - intellectual deficit - deafness - hypogenitalism (Orphanet:3085)
Rosaï-Dorfman disease (Orphanet:158014)
TESTES, RUDIMENTARY (OMIM:273150)
Wolfram syndrome 1 (OMIM:222300)
Woodhouse-Sakati syndrome (Orphanet:3464)
Xq27.3q28 duplication syndrome (Orphanet:261483)