Hypogonadism

Symptom Information:

Symptom ID: HPO:0000135
Synonyms:
Hypogonadism (disorder) [Orphanet:41780]
Hypogonadism [Orphanet:41780]
Hypogonadism [OMIM:Hypogonadism]
Late puberty/hypogonadism/hypogenitalism [Orphanet:41780]
Hypogonadism [MedDRA:10058359]
Gonadal insufficiency [MedDRA:10058359]
Hypogonadism (1 patient) [OMIM:Hypogonadism (1 patient)]
Hypogonadism (in contiguous gene syndrome patients) [OMIM:Hypogonadism (in contiguous gene syndrome patients)]
Hypogonadism (in males) [OMIM:Hypogonadism (in males)]
Hypogonadism (less common) [OMIM:Hypogonadism (less common)]
Hypogonadism (major) [OMIM:Hypogonadism (major)]
Hypogonadism (reported in 1 patient) [OMIM:Hypogonadism (reported in 1 patient)]
Quality:
Cross references:
Orphanet:41780 "Late puberty/hypogonadism/hypogenitalism" [Orphanet:41780]
OMIM: "Hypogonadism" [OMIM:Hypogonadism]
OMIM: "Hypogonadism (1 patient)" [OMIM:Hypogonadism (1 patient)]
OMIM: "Hypogonadism (in contiguous gene syndrome patients)" [OMIM:Hypogonadism (in contiguous gene syndrome patients)]
OMIM: "Hypogonadism (in males)" [OMIM:Hypogonadism (in males)]
OMIM: "Hypogonadism (less common)" [OMIM:Hypogonadism (less common)]
OMIM: "Hypogonadism (major)" [OMIM:Hypogonadism (major)]
OMIM: "Hypogonadism (reported in 1 patient)" [OMIM:Hypogonadism (reported in 1 patient)]
UMLS:C0020619 "Hypogonadism" [HPO:0000135]
UMLS:C0020619 "Hypogonadism" [Orphanet:41780]
Is a (Direct Parents):
HPO         Puberty and gonadal disorders
Orphanet Abnormality of the endocrine system
HPO         Abnormality of reproductive system physiology
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)
       Abnormality of the genitourinary system(HPO:0000119)
          Abnormality of the genital system(HPO:0000078)
             Abnormality of reproductive system physiology(HPO:0000080)
                Hypogonadism(HPO:0000135)
MedDRA:
Endocrine disorders(MedDRA:10014698)
    Endocrine disorders of gonadal function(MedDRA:10014701)
       Endocrine abnormalities of gonadal function NEC(MedDRA:10014691)
          Hypogonadism(HPO:0000135)
Database Frequency: 89 / 7739
Resource:

All diseases associated with this symptom:

2p15p16.1 microdeletion syndrome (Orphanet:261349)
48,XXYY syndrome (Orphanet:10)
ACRODYSOSTOSIS 1 WITH OR WITHOUT HORMONE RESISTANCE (OMIM:101800)
ALG1-CDG (Orphanet:79327)
ANE syndrome (Orphanet:157954)
ATAXIA-TELANGIECTASIA (OMIM:208900)
Acrodermatitis enteropathica, zinc deficiency type (Orphanet:37)
Acrodysostosis with multiple hormone resistance (Orphanet:280651)
Albright hereditary osteodystrophy (Orphanet:665)
Alström syndrome (Orphanet:64)
Arrhinia - choanal atresia - microphthalmia (Orphanet:1135)
Autoimmune polyendocrinopathy type 1 (Orphanet:3453)
Bangstad syndrome (Orphanet:1227)
Bardet-Biedl syndrome (Orphanet:110)
Bardet-Biedl syndrome 1 (OMIM:209900 )
Bardet-Biedl syndrome 10 (OMIM:615987)
Bardet-Biedl syndrome 11 (OMIM:615988)
Bardet-Biedl syndrome 12 (OMIM:615989)
Bardet-Biedl syndrome 17 (OMIM:615994)
Bardet-Biedl syndrome 2 (OMIM:615981)
Bardet-Biedl syndrome 4 (OMIM:615982)
Bardet-Biedl syndrome 5 (OMIM:615983)
Bardet-Biedl syndrome 7 (OMIM:615984)
Bardet-Biedl syndrome 8 (OMIM:615985)
Björnstad syndrome (Orphanet:123)
Brachytelephalangic chondrodysplasia punctata (Orphanet:79345)
CHONDRODYSPLASIA PUNCTATA 1, X-LINKED RECESSIVE (OMIM:302950)
COCKAYNE SYNDROME A (OMIM:216400)
CONE-ROD DYSTROPHY 1 (OMIM:600624)
Cabezas syndrome (Orphanet:85293)
Carpenter-Waziri syndrome (Orphanet:93973)
Chudley-Lowry-Hoar syndrome (Orphanet:93971)
Colobomatous microphthalmia-obesity-hypogenitalism-intellectual disability syndrome (Orphanet:363741)
Congenital muscular dystrophy - infantile cataract - hypogonadism (Orphanet:1875)
Cystinosis (Orphanet:213)
DEAFNESS, CONDUCTIVE, WITH MALFORMED EXTERNAL EAR (OMIM:221300)
DEAFNESS, CONGENITAL, WITH TOTAL ALBINISM (OMIM:220900)
GYNECOMASTIA, FAMILIAL (OMIM:306500)
HYPOGONADOTROPIC HYPOGONADISM 18 WITH OR WITHOUT ANOSMIA (OMIM:615267)
HYPOGONADOTROPIC HYPOGONADISM 20 WITH OR WITHOUT ANOSMIA (OMIM:615270)
HYPOGONADOTROPIC HYPOGONADISM 22 WITH OR WITHOUT ANOSMIA (OMIM:616030)
HYPOGONADOTROPIC HYPOGONADISM 3 WITH OR WITHOUT ANOSMIA (OMIM:244200)
Hemochromatosis type 2 (Orphanet:79230)
Hemochromatosis type 3 (Orphanet:225123)
Hemochromatosis, type 2B (OMIM:613313)
Holmes-Gang syndrome (Orphanet:93970)
Hypergonadotropic hypogonadism - cataract syndrome (Orphanet:2410)
Insulin-resistance syndrome type A (Orphanet:2297)
Intellectual deficit - balding - patella luxation - acromicria (Orphanet:3041)
Juberg-Marsidi syndrome (Orphanet:93972)
MELAS (Orphanet:550)
MERRF (Orphanet:551)
Mandibular hypoplasia-deafness-progeroid syndrome (Orphanet:363649)
Mitochondrial myopathy and sideroblastic anemia (Orphanet:2598)
Noonan syndrome (Orphanet:648)
Obesity due to congenital leptin deficiency (Orphanet:66628)
Odontotrichomelic syndrome (Orphanet:2723)
PITUITARY HORMONE DEFICIENCY, COMBINED, 2 (OMIM:262600)
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 3 (OMIM:609286)
Panhypopituitarism (Orphanet:90695)
Partial androgen insensitivity syndrome (Orphanet:90797)
Primary hypergonadotropic hypogonadism - partial alopecia (Orphanet:2232)
Primary microcephaly-epilepsy-permanent neonatal diabetes syndrome (Orphanet:306558)
Proximal myotonic myopathy (Orphanet:606)
Pseudohypoparathyroidism type 1A (Orphanet:79443)
Pseudohypoparathyroidism type 1C (Orphanet:79444)
RETINOPATHY, PIGMENTARY, AND MENTAL RETARDATION (OMIM:268050)
Renier-Gabreels-Jasper syndrome (Orphanet:93975)
Richards-Rundle syndrome (Orphanet:1399)
Rothmund-Thomson syndrome (Orphanet:2909)
SCHAAF-YANG SYNDROME (OMIM:615547)
Say-Barber-Miller syndrome (Orphanet:3132)
Senior-Loken syndrome 9 (OMIM:616629)
Severe congenital hypochromic anemia with ringed sideroblasts (Orphanet:300298)
Smith-Fineman-Myers syndrome (Orphanet:93974)
Spastic paraparesis - deafness (Orphanet:2815)
Steinert myotonic dystrophy (Orphanet:273)
TRICHOTHIODYSTROPHY, PHOTOSENSITIVE (OMIM:601675)
WAARDENBURG SYNDROME, TYPE 4C (OMIM:613266)
Werner syndrome (Orphanet:902)
Wilson-Turner syndrome (Orphanet:3459)
Wolfram syndrome (Orphanet:3463)
Wolfram syndrome 1 (OMIM:222300)
Wolfram syndrome 2 (OMIM:604928)
Woodhouse-Sakati syndrome (Orphanet:3464)
X-linked cerebral adrenoleukodystrophy (Orphanet:139396)
X-linked intellectual deficit - hypotonic face (Orphanet:73220)
Xeroderma pigmentosum complementation group B (Orphanet:276252)
Xq27.3q28 duplication syndrome (Orphanet:261483)