hypogonadism - CISMeF

Preferred Label : hypogonadism;

MeSH 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).;

MeSH hyponym : hypogonadotropic hypogonadism; hypergonadotropic hypogonadism; hypogonadism, isolated hypogonadotropic; Hypogonadism, Hypogonadotropic; Hypogonadism, Hypergonadotropic;

MeSH annotation : for male or female; do not routinely interpret hypogonadism in male as EUNUCHISM: use terminology of author;

Wikipedia link : https://en.wikipedia.org/wiki/Hypogonadism;

Details

Origin ID

D007006;

UMLS CUI

C0020619;

ATC code(s)
- fluoxymesterone [ATC Code]
Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Gonadotrophin deficiency [MedDRA Preferred Term]
- Gonadotropin deficiency [ICD-11 Subcategory]
- Hypergonadotropic hypogonadism [PASCAL descriptor]
- Hypergonadotropic hypogonadism [HPO term]
- Hypergonadotropic hypogonadism [MedDRA LLT]
- Hypogonadotrophic hypogonadism [MedDRA LLT]
- Hypogonadotropic hypogonadism [PASCAL descriptor]
- Hypogonadotropic hypogonadism [HPO term]
- Hypogonadotropic hypogonadism (disorder) [SNOMED CT concept]
- Hypogonadotropic hypogonadism 7 with or without anosmia [OMIM Phenotype]
- Hypopituitarism [ICD-10 Sub-category]
- Hypopituitarism [ICD-10 Sub-category (who)]
- Klinefelter Syndrome [NCIt concept]
- Klinefelter syndrome [DO Concept]
- hypogonadotropic hypogonadism [SNOMED Notion]
- primary ovarian insufficiency [DO Concept]
Currated CISMeF NLP mapping
- Hypogonadism [PASCAL descriptor]
- Hypogonadism [HPO term]
- Hypogonadism [MedDRA Preferred Term]
- Hypogonadism [NCIt concept]
- Hypogonadism (disorder) [SNOMED CT concept]
- hypogonadism [Disease (Nov.)]
- hypogonadism [DO Concept]
- hypogonadism, nos [SNOMED Notion]
DO Cross reference
- hypogonadism [DO Concept]
HPO term
- Gonadotropin deficiency [HPO term]
- Hypergonadotropic hypogonadism [HPO term]
- Hypogonadism [HPO term]
- Hypogonadotropic hypogonadism [HPO term]
Record concept(s)
- hypergonadotropic hypogonadism [MeSH concept]
- hypogonadism [MeSH concept]
- hypogonadism, isolated hypogonadotropic [MeSH concept]
- hypogonadotropic hypogonadism [MeSH concept]
Related MeSH Supplementary Concept(s)
- Alopecia-Mental retardation syndrome with convulsions and hypergonadotropic hypogonadism [MeSH Supplementary Concept]
- Borjeson-Forssman-Lehmann syndrome [MeSH Supplementary Concept]
- Chudley-Rozdilsky syndrome [MeSH Supplementary Concept]
- Deafness-Hypogonadism syndrome [MeSH Supplementary Concept]
- MEHMO syndrome [MeSH Supplementary Concept]
- Richards-Rundle syndrome [MeSH Supplementary Concept]
- alopecia hypogonadism extrapyramidal disorder [MeSH Supplementary Concept]
- bassoe syndrome [MeSH Supplementary Concept]
- biemond syndrome II [MeSH Supplementary Concept]
- cantalamessa baldini ambrosi syndrome [MeSH Supplementary Concept]
- cardiomyopathy hypogonadism collagenoma syndrome [MeSH Supplementary Concept]
- cerebellar ataxia and hypergonadotropic hypogonadism [MeSH Supplementary Concept]
- cerebellar ataxia and hypogonadotropic hypogonadism [MeSH Supplementary Concept]
- chang davidson carlson syndrome [MeSH Supplementary Concept]
- chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism [MeSH Supplementary Concept]
- de Sanctis-Cacchione syndrome [MeSH Supplementary Concept]
- encephalopathy, spastic tetraparesis, and hypogonadism [MeSH Supplementary Concept]
- gonadal dysgenesis, hypergonadotropic, XX type, short stature, and recurrent metabolic acidosis [MeSH Supplementary Concept]
- hypergonadotropic hypogonadism and partial alopecia [MeSH Supplementary Concept]
- hypogonadism and testicular atrophy [MeSH Supplementary Concept]
- hypogonadism with Low-Grade mental deficiency and microcephaly [MeSH Supplementary Concept]
- hypogonadism, male, with mental retardation and skeletal anomalies [MeSH Supplementary Concept]
- ichthyosis and male hypogonadism [MeSH Supplementary Concept]
- idiopathic hypogonadotropic hypogonadism [MeSH Supplementary Concept]
- johnson neuroectodermal syndrome [MeSH Supplementary Concept]
- leukodystrophy, hypomyelinating, with hypodontia and hypogonadotropic hypogonadism [MeSH Supplementary Concept]
- lubinsky syndrome [MeSH Supplementary Concept]
- malouf syndrome [MeSH Supplementary Concept]
- martsolf syndrome [MeSH Supplementary Concept]
- mental retardation-hypotonic facies syndrome, x-linked, 1 [MeSH Supplementary Concept]
- mineralocorticoid deficiency, isolated [MeSH Supplementary Concept]
- moebius axonal neuropathy hypogonadism [MeSH Supplementary Concept]
- muscular dystrophy, congenital, infantile with cataract and hypogonadism [MeSH Supplementary Concept]
- myopathy, cataract, hypogonadism syndrome [MeSH Supplementary Concept]
- progressive external ophthalmoplegia with hypogonadism [MeSH Supplementary Concept]
- retinitis pigmentosa, deafness, mental retardation, and hypogonadism [MeSH Supplementary Concept]
- rud syndrome [MeSH Supplementary Concept]
- scholte syndrome [MeSH Supplementary Concept]
- seemanova lesny syndrome [MeSH Supplementary Concept]
- slti salem syndrome [MeSH Supplementary Concept]
- vasquez hurst sotos syndrome [MeSH Supplementary Concept]
- warburg sjo fledelius syndrome [MeSH Supplementary Concept]
- weinstein kliman scully syndrome [MeSH Supplementary Concept]
- woodhouse sakati syndrome [MeSH Supplementary Concept]
- young hughes syndrome [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hypogonadism [HPO term]
- Hypogonadism [MedDRA Preferred Term]
- Hypogonadism [PASCAL descriptor]
- Hypogonadism [NCIt concept]
- Hypogonadism (disorder) [SNOMED CT concept]
- hypogonadism [DO Concept]
- hypogonadism [Disease (Nov.)]
- hypogonadism, nos [SNOMED Notion]
Validated automatic mappings to BTNT
- Hypergonadotropic Hypogonadism [NCIt concept]
- Hypogonadotropic Hypogonadism [NCIt concept]
- Isolated Hypogonadotropic Hypogonadism [NCIt concept]
- Primary hypogonadism (disorder) [SNOMED CT concept]
- hypergonadotropic hypogonadism [Disease (Nov.)]
- hypogonadotropic hypogonadism [DO Concept]
- hypogonadotropic hypogonadism [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

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