TERMIUM Plus®
The Government of Canada’s terminology and linguistic data bank.
HYPOGONADISM [7 records]
Record 1 - internal organization data 2019-12-05
Record 1, English
Record 1, Subject field(s)
- Human Diseases - Various
- Genetics
Record 1, Main entry term, English
- Prader–Willi syndrome
1, record 1, English, Prader%26ndash%3BWilli%20syndrome
correct
Record 1, Abbreviations, English
- PWS 2, record 1, English, PWS
correct
Record 1, Synonyms, English
Record 1, Textual support, English
Record number: 1, Textual support number: 1 DEF
A congenital disorder characterized by obesity, short stature, lack of muscle tone, hypogonadism, and central nervous system dysfunction[, which is caused] by loss of expression of genes on paternally derived chromosome 15q11-q13, usually as a result of a deletion... 3, record 1, English, - Prader%26ndash%3BWilli%20syndrome
Record 1, French
Record 1, Domaine(s)
- Maladies humaines diverses
- Génétique
Record 1, Main entry term, French
- syndrome de Prader-Willi
1, record 1, French, syndrome%20de%20Prader%2DWilli
correct, masculine noun
Record 1, Abbreviations, French
- SPW 1, record 1, French, SPW
correct, masculine noun
Record 1, Synonyms, French
Record 1, Textual support, French
Record number: 1, Textual support number: 1 CONT
Le syndrome de Prader-Willi (SPW) est une maladie génétique complexe due à un défaut d'expression des gènes de la région du chromosome 15q11-q13 d'origine paternelle. Le syndrome associe : une hypotonie néonatale sévère, l'apparition précoce d'une obésité morbide associée à une hyperphagie, une petite taille, un hypogonadisme, des troubles d'apprentissage, des problèmes de comportement et des troubles psychiatriques. 2, record 1, French, - syndrome%20de%20Prader%2DWilli
Record 1, Spanish
Record 1, Textual support, Spanish
Record 2 - internal organization data 2012-02-17
Record 2, English
Record 2, Subject field(s)
- The Genitals
Record 2, Main entry term, English
- Kallmann’s syndrome
1, record 2, English, Kallmann%26rsquo%3Bs%20syndrome
correct
Record 2, Abbreviations, English
Record 2, Synonyms, English
- hypogonadism with anosmia 1, record 2, English, hypogonadism%20with%20anosmia
correct
- Kallmann syndrome 2, record 2, English, Kallmann%20syndrome
correct
- olfactory genital dysplasia 2, record 2, English, olfactory%20genital%20dysplasia
correct
Record 2, Textual support, English
Record number: 2, Textual support number: 1 DEF
Hereditary hypogonadotropic hypogonadism in males, associated with hyposmia or anosmia due to agenesis of the olfactory lobes. 2, record 2, English, - Kallmann%26rsquo%3Bs%20syndrome
Record 2, French
Record 2, Domaine(s)
- Organes génitaux
Record 2, Main entry term, French
- dysplasie olfactogénitale
1, record 2, French, dysplasie%20olfactog%C3%A9nitale
correct, feminine noun
Record 2, Abbreviations, French
Record 2, Synonyms, French
- syndrome de Morsier-Kallmann 1, record 2, French, syndrome%20de%20Morsier%2DKallmann
masculine noun
- dysplasie olfacto-génitale 1, record 2, French, dysplasie%20olfacto%2Dg%C3%A9nitale
correct, feminine noun
- syndrome de Morsier 1, record 2, French, syndrome%20de%20Morsier
correct, masculine noun
Record 2, Textual support, French
Record number: 2, Textual support number: 1 OBS
hypogonadisme : insuffisance de sécrétion des glandes génitales. 1, record 2, French, - dysplasie%20olfactog%C3%A9nitale
Record 2, Spanish
Record 2, Textual support, Spanish
Record 3 - internal organization data 2012-01-30
Record 3, English
Record 3, Subject field(s)
- Genitourinary Tract
- Biotechnology
Record 3, Main entry term, English
- hypogonadism
1, record 3, English, hypogonadism
correct
Record 3, Abbreviations, English
Record 3, Synonyms, English
- hypogonadia 2, record 3, English, hypogonadia
- hypogenitalism 3, record 3, English, hypogenitalism
Record 3, Textual support, English
Record number: 3, Textual support number: 1 DEF
A condition resulting from or characterized by abnormally decreased functional activity of the gonads, with retardation of growth and sexual development. 4, record 3, English, - hypogonadism
Record number: 3, Textual support number: 2 DEF
Diminished hormonal or reproductive functioning in the testes or the ovaries. 2, record 3, English, - hypogonadism
Record 3, French
Record 3, Domaine(s)
- Appareil génito-urinaire
- Biotechnologie
Record 3, Main entry term, French
- hypogonadisme
1, record 3, French, hypogonadisme
correct, masculine noun
Record 3, Abbreviations, French
Record 3, Synonyms, French
- hypogénitalisme 2, record 3, French, hypog%C3%A9nitalisme
correct, masculine noun
Record 3, Textual support, French
Record number: 3, Textual support number: 1 DEF
Insuffisance de fonctionnement des gonades. 3, record 3, French, - hypogonadisme
Record 3, Spanish
Record 3, Campo(s) temático(s)
- Aparato genitourinario
- Biotecnología
Record 3, Main entry term, Spanish
- hipogonadismo
1, record 3, Spanish, hipogonadismo
correct, masculine noun
Record 3, Abbreviations, Spanish
Record 3, Synonyms, Spanish
Record 3, Textual support, Spanish
Record 4 - internal organization data 2011-03-17
Record 4, English
Record 4, Subject field(s)
- Genetics
Record 4, Main entry term, English
- Steinert’s disease 1, record 4, English, Steinert%26rsquo%3Bs%20disease
Record 4, Abbreviations, English
Record 4, Synonyms, English
- Batten’s disease 1, record 4, English, Batten%26rsquo%3Bs%20disease
- Batten-Steinert syndrome 1, record 4, English, Batten%2DSteinert%20syndrome
- Curschmann-Batten-Steinert syndrome 1, record 4, English, Curschmann%2DBatten%2DSteinert%20syndrome
- Curschmann-Steinert syndrome 1, record 4, English, Curschmann%2DSteinert%20syndrome
- myotonia atrophica 1, record 4, English, myotonia%20atrophica
- atrophic myotonia 1, record 4, English, atrophic%20myotonia
- myotonic dystrophy 1, record 4, English, myotonic%20dystrophy
- dystrophia myotonica 1, record 4, English, dystrophia%20myotonica
Latin
Record 4, Textual support, English
Record number: 4, Textual support number: 1 DEF
A rare, slowly progressive hereditary disease transmitted as an autosomal dominant trait, characterized by myotonia followed by atrophy of the muscles(especially those of the face and neck), cataracts, hypogonadism, frontal balding, and cardiac abnormalities. 1, record 4, English, - Steinert%26rsquo%3Bs%20disease
Record 4, French
Record 4, Domaine(s)
- Génétique
Record 4, Main entry term, French
- maladie de Steinert
1, record 4, French, maladie%20de%20Steinert
feminine noun
Record 4, Abbreviations, French
Record 4, Synonyms, French
- atrophie myotonique 1, record 4, French, atrophie%20myotonique
feminine noun
- dystrophie myotonique 1, record 4, French, dystrophie%20myotonique
- myopathie atrophique avec myotonie 1, record 4, French, myopathie%20atrophique%20avec%20myotonie
feminine noun
- myopathie myotonique 1, record 4, French, myopathie%20myotonique
- myotonie atrophique 1, record 4, French, myotonie%20atrophique
feminine noun
- myotonie dystrophique 1, record 4, French, myotonie%20dystrophique
masculine noun
- syndrome de Batten Steinert 1, record 4, French, syndrome%20de%20Batten%20Steinert
masculine noun
- syndrome de Curschmann-Batten-Steinert 1, record 4, French, syndrome%20de%20Curschmann%2DBatten%2DSteinert
- dystrophia myotonica 1, record 4, French, dystrophia%20myotonica
Latin
Record 4, Textual support, French
Record number: 4, Textual support number: 1 DEF
Affection héréditaire à transmission autosomique dominante, caractérisée par une atrophie musculaire extrême atteignant la face et l'extrémité distale des membres, associée à une myotonie modérée. Les troubles dystrophiques ne sont pas seulement limités au tissu musculaire, mais peuvent aussi atteindre les cheveux (alopécie), le cristallin (cataracte) et les gonades. 1, record 4, French, - maladie%20de%20Steinert
Record number: 4, Textual support number: 1 CONT
Quant aux complications testiculaires de la myopathie myotonique (maladie de Steinert), elles sont tardives et précédées d'une période de fertilité. 1, record 4, French, - maladie%20de%20Steinert
Record 4, Spanish
Record 4, Textual support, Spanish
Record 5 - internal organization data 2011-02-18
Record 5, English
Record 5, Subject field(s)
- Chemical Elements and Compounds
- Medication
Universal entry(ies) Record 5
Record 5, Main entry term, English
- fluoximesterone
1, record 5, English, fluoximesterone
correct
Record 5, Abbreviations, English
Record 5, Synonyms, English
Record 5, Textual support, English
Record number: 5, Textual support number: 1 OBS
An anabolic steroid that has been used in the treatment of male hypogonadism, delayed puberty in males, and in the treatment of breast neoplasms in women. 2, record 5, English, - fluoximesterone
Record number: 5, Textual support number: 2 OBS
Chemical formula: C20H29FO3 3, record 5, English, - fluoximesterone
Record 5, French
Record 5, Domaine(s)
- Éléments et composés chimiques
- Médicaments
Entrée(s) universelle(s) Record 5
Record 5, Main entry term, French
- fluoximestérone
1, record 5, French, fluoximest%C3%A9rone
correct, feminine noun
Record 5, Abbreviations, French
Record 5, Synonyms, French
Record 5, Textual support, French
Record number: 5, Textual support number: 1 OBS
Formule chimique : C20H29FO3 2, record 5, French, - fluoximest%C3%A9rone
Record 5, Spanish
Record 5, Campo(s) temático(s)
- Elementos y compuestos químicos
- Medicamentos
Entrada(s) universal(es) Record 5
Record 5, Main entry term, Spanish
- fluoximesterona
1, record 5, Spanish, fluoximesterona
feminine noun
Record 5, Abbreviations, Spanish
Record 5, Synonyms, Spanish
Record 5, Textual support, Spanish
Record number: 5, Textual support number: 1 OBS
Fórmula química: C20H29FO3 2, record 5, Spanish, - fluoximesterona
Record 6 - internal organization data 2000-05-15
Record 6, English
Record 6, Subject field(s)
- Diagnostic Procedures (Medicine)
Record 6, Main entry term, English
- Bardet-Biedl syndrome
1, record 6, English, Bardet%2DBiedl%20syndrome
correct
Record 6, Abbreviations, English
Record 6, Synonyms, English
- Laurence-Moon-Biedl syndrome 2, record 6, English, Laurence%2DMoon%2DBiedl%20syndrome
- Moon-Bardet-Biedl syndrome 2, record 6, English, Moon%2DBardet%2DBiedl%20syndrome
Record 6, Textual support, English
Record number: 6, Textual support number: 1 DEF
An autosomal recessive disorder characterized by mental retardation, pigmentary retinopathy, obesity, polydactyly and hypogonadism. 3, record 6, English, - Bardet%2DBiedl%20syndrome
Record 6, French
Record 6, Domaine(s)
- Méthodes diagnostiques (Médecine)
Record 6, Main entry term, French
- syndrome de Bardet-Biedl
1, record 6, French, syndrome%20de%20Bardet%2DBiedl
correct, masculine noun
Record 6, Abbreviations, French
Record 6, Synonyms, French
- syndrome de Laurence-Moon-Bardet-Biedl 2, record 6, French, syndrome%20de%20Laurence%2DMoon%2DBardet%2DBiedl
masculine noun
- syndrome de Moon-Bardet-Biedl 2, record 6, French, syndrome%20de%20Moon%2DBardet%2DBiedl
masculine noun
Record 6, Textual support, French
Record number: 6, Textual support number: 1 DEF
Affectation autosomale récessive caractérisée par une rétinopathie pigmentaire, une obésité, un hypogonadisme, une polydactylie et un retard mental. 3, record 6, French, - syndrome%20de%20Bardet%2DBiedl
Record number: 6, Textual support number: 1 OBS
Source MVISI-F : Le nouveau dictionnaire de la vision par Michel Millodot, Médiacom Vision Éditeur, 1997. 4, record 6, French, - syndrome%20de%20Bardet%2DBiedl
Record 6, Spanish
Record 6, Textual support, Spanish
Record 7 - internal organization data 1981-04-21
Record 7, English
Record 7, Subject field(s)
- Histology
Record 7, Main entry term, English
- Reifensteins’s syndrome 1, record 7, English, Reifensteins%26rsquo%3Bs%20syndrome
Record 7, Abbreviations, English
Record 7, Synonyms, English
- hereditary familial hypogonadism 1, record 7, English, hereditary%20familial%20hypogonadism
Record 7, Textual support, English
Record number: 7, Textual support number: 1 DEF
A syndrome of familial male pseudohermaphrodism associated with hypospadias, primary hypogonadism, postpubertal testicular atrophy and azoospermia; signs of testosterone deficiency, and often gynecomastia. 1, record 7, English, - Reifensteins%26rsquo%3Bs%20syndrome
Record number: 7, Textual support number: 1 CONT
A complete Reifenstein syndrome with dysgenetic lesions of the seminiferous tubes and ambiguous genitals (short penis with hypospadias) as well as a deficiency in virility would be the maximal expression of the lesion. 1, record 7, English, - Reifensteins%26rsquo%3Bs%20syndrome
Record 7, French
Record 7, Domaine(s)
- Histologie
Record 7, Main entry term, French
- syndrome de Reinfenstein
1, record 7, French, syndrome%20de%20Reinfenstein
masculine noun
Record 7, Abbreviations, French
Record 7, Synonyms, French
- hypogonadisme familial héréditaire 1, record 7, French, hypogonadisme%20familial%20h%C3%A9r%C3%A9ditaire
masculine noun
Record 7, Textual support, French
Record number: 7, Textual support number: 1 DEF
Malformation testiculaire congénitale et héréditaire [...] caractérisée par une atrophie post-pubertaire des tubes séminifères, une azoospermie et un degré variable d'eunuchoïsme, associés à un hypospadias. Le caryotype est normal, de type XY, dans tous les tissus, ce qui distingue ce syndrome de celui de Klinefelter. 1, record 7, French, - syndrome%20de%20Reinfenstein
Record number: 7, Textual support number: 1 CONT
Le pseudo-hermaphrodisme masculin peut reconnaître une origine génique comme dans la féminisation testiculaire ou le syndrome de Reifenstein. 1, record 7, French, - syndrome%20de%20Reinfenstein
Record 7, Spanish
Record 7, Textual support, Spanish
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