Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandGonadal Disorders (D006058)
..Starting node
..expandHypogonadism (D007006)

       Child Nodes:
........expandAlopecia hypogonadism extrapyramidal disorder (C537053)
........expandAlopecia-Mental Retardation Syndrome with Convulsions and Hypergonadotropic Hypogonadism (C563370)
........expandBassoe syndrome (C537661)
........expandBiemond syndrome type 2 (C535439)
........expandBorjeson-Forssman-Lehmann syndrome (C536575)
........expandCantalamessa Baldini Ambrosi syndrome (C537981)
........expandCardiomyopathy hypogonadism collagenoma syndrome (C535582)
........expandCerebellar Ataxia and Hypergonadotropic Hypogonadism (C565308)
........expandCerebellar Ataxia and Hypogonadotropic Hypogonadism (C565870)
........expandChang Davidson Carlson syndrome (C538075)
........expandChorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism (C565850)
........expandChudley-Rozdilsky syndrome (C535458)
........expandDe Sanctis-Cacchione syndrome (C535992)
........expandDeafness-Hypogonadism Syndrome (C564435)
........expandEncephalopathy, Spastic Tetraparesis, and Hypogonadism (C565722)
........expandEunuchism (D005058) Child2
........expandGonadal Dysgenesis, Hypergonadotropic, XX Type, Short Stature, and Recurrent Metabolic Acidosis (C565295)
........expandHypergonadotropic Hypogonadism And Partial Alopecia (C567109)
........expandHypogonadism and Testicular Atrophy (C567108)
........expandHypogonadism with Low-Grade Mental Deficiency and Microcephaly (C565482)
........expandHypogonadism, Male, With Mental Retardation And Skeletal Anomalies (C564406)
........expandIchthyosis and male hypogonadism (C537365)
........expandIdiopathic Hypogonadotropic Hypogonadism (C562785)
........expandJohnson neuroectodermal syndrome (C535882)
........expandKallmann Syndrome (D017436) Child9
........expandKlinefelter Syndrome (D007713)
........expandLeukodystrophy, Hypomyelinating, with Hypodontia and Hypogonadotropic Hypogonadism (C567313)
........expandLubinsky syndrome (C543092)
........expandMalouf syndrome (C535703)
........expandMartsolf syndrome (C536028)
........expandMEHMO syndrome (C537451)
........expandMENTAL RETARDATION, X-LINKED, WITH SHORT STATURE, HYPOGONADISM, AND ABNORMAL GAIT (OMIM:300354)
........expandMental retardation-hypotonic facies syndrome, x-linked, 1 (C537457)
........expandMineralocorticoid Deficiency, Isolated (C567596)
........expandMoebius axonal neuropathy hypogonadism (C535806)
........expandMOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM, AND FACIAL DYSMORPHISM (OMIM:300845)
........expandMuscular dystrophy, congenital, infantile with cataract and hypogonadism (C537385)
........expandMyopathy, Cataract, Hypogonadism Syndrome (C563578)
........expandProgressive External Ophthalmoplegia With Hypogonadism (C563576)
........expandRetinitis Pigmentosa, Deafness, Mental Retardation, and Hypogonadism (C564841)
........expandRichards-Rundle syndrome (C535674)
........expandRud Syndrome (C535878)
........expandScholte syndrome (C536638)
........expandSeemanova Lesny syndrome (C537536)
........expandSexual Infantilism (D050035)
........expandSlti Salem syndrome (C536673)
........expandVasquez Hurst Sotos syndrome (C536533)
........expandWarburg Sjo Fledelius syndrome (C536681)
........expandWeinstein Kliman Scully syndrome (C536688)
........expandWoodhouse Sakati syndrome (C536742)
........expandYoung Hughes syndrome (C536715)



 Sister Nodes: 
..expandDisorders of Sex Development (D012734) Child107
..expandFemale Athlete Triad Syndrome (D053716)
..expandHypogonadism (D007006) Child62
..expandOvarian Diseases (D010049) Child51
..expandPuberty, Delayed (D011628) Child1
..expandPuberty, Precocious (D011629) Child8
..expandTesticular Diseases (D013733) Child28
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:5567
Name:Hypogonadism
Definition:Condition resulting from deficient gonadal functions, such as GAMETOGENESIS and the production of GONADAL STEROID HORMONES. It is characterized by delay in GROWTH, germ cell maturation, and development of secondary sex characteristics. Hypogonadism can be due to a deficiency of GONADOTROPINS (hypogonadotropic hypogonadism) or due to primary gonadal failure (hypergonadotropic hypogonadism).
Alternative IDs:
ParentIDs:MESH:D006058
TreeNumbers:C19.391.482
Synonyms:Hypergonadotropic Hypogonadism |Hypogonadism, Hypergonadotropic |Hypogonadism, Hypogonadotropic |Hypogonadism, Isolated Hypogonadotropic |Hypogonadotropic Hypogonadism
Slim Mappings:Endocrine system disease
Reference: MedGen: D007006
MeSH: D007006
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants