01
- Entity Type
- Diseases
- Relation Groups
- 2
- Relation Preview
- 16
Basic Information
Grouped by core information, identifiers, and descriptions.
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Core Information
- Disease Name
- Hypogonadism
- Standard Disease Name
- hypogonadism
- MeSH Tree
- No data
- ICD-10
- No data
Identifiers
- DO ID
- No data
- MeSH ID
- D007006
- OMIM ID
- MTHU000132
- UMLS ID
- C0020619
- HPO ID
- No data
Description and Extensions
- Description
- NCI2016_02D:A disorder characterized by decreased function of the gonads. Clinical manifestations in both males and females include poor libido, infertility, and osteoporosis. Additional signs in males include erectile dysfunction, muscle atrophy, gynecomastia and increased abdominal fat. In females, additional signs include shrinking of the breasts and loss of, or failure to develop menstruation.|MSH2017_2016_08_12: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).|HPO2016_07_04:A decreased functionality of the gonad. [HPO:curators]|CSP2006:condition resulting from or characterized by abnormally decreased functional activity of the gonads, with retardation of growth and sexual development.