17β-Hydroxysteroid dehydrogenase III deficiency
17β-Hydroxysteroid dehydrogenase III deficiency is a rare autosomal recessive disorder of sexual development, or intersex condition, affecting testosterone biosynthesis by 17β-hydroxysteroid dehydrogenase III (17β-HSD III), which can produce impaired virilization (historically termed male pseudohermaphroditism) of genetically male infants.
17-beta-hydroxysteroid dehydrogenase III deficiency17-beta-hydroxysteroid dehydrogenase X deficiency17-beta-hydroxysteroid dehydrogenase deficiency17-beta-hydroxysteroid dehydrogenase deficiency III17BHDD17 beta hydroxysteroide dehydrogenase deficiency17β-HSD3 deficiency17β-HSDIII deficiency17β-HSD 3 deficiency17β-HSD III deficiency17β-HSD type 3 deficiency17β-HSD type III deficiency17β-Hydroxysteroid dehydrogenase 3 deficiency17β-Hydroxysteroid dehydrogenase deficiency17β-Hydroxysteroid dehydrogenase type 3 deficiency17β-Hydroxysteroid dehydrogenase type III deficiency17β-hydroxysteroid dehydrogenase 3 deficiency17β-hydroxysteroid dehydrogenase III deficiency17β-hydroxysteroid dehydrogenase deficiency17β-hydroxysteroid dehydrogenase type 3 deficiency17β-hydroxysteroid dehydrogenase type III deficiencyMale pseudohermaphroditism due to 17-beta-hydroxysteroid dehydrogenase deficiency
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17-beta-hydroxysteroid dehydrogenase III deficiency17-beta-hydroxysteroid dehydrogenase X deficiency17-beta-hydroxysteroid dehydrogenase deficiency17-beta-hydroxysteroid dehydrogenase deficiency III17BHDD17 beta hydroxysteroide dehydrogenase deficiency17β-HSD3 deficiency17β-HSDIII deficiency17β-HSD 3 deficiency17β-HSD III deficiency17β-HSD type 3 deficiency17β-HSD type III deficiency17β-Hydroxysteroid dehydrogenase17β-Hydroxysteroid dehydrogenase 3 deficiency17β-Hydroxysteroid dehydrogenase deficiency17β-Hydroxysteroid dehydrogenase type 3 deficiency17β-Hydroxysteroid dehydrogenase type III deficiency17β-hydroxysteroid dehydrogenase 3 deficiency17β-hydroxysteroid dehydrogenase III deficiency17β-hydroxysteroid dehydrogenase deficiency17β-hydroxysteroid dehydrogenase type 3 deficiency17β-hydroxysteroid dehydrogenase type III deficiencyAndrogen insensitivity syndromeDisorders of sex developmentFollicle-stimulating hormone insensitivityInborn errors of steroid metabolismIntersex and LGBTIntersex rights in AustraliaLeydig cell hypoplasiaList of OMIM disorder codesList of diseases (0–9)List of diseases (M)Male pseudohermaphroditism due to 17-beta-hydroxysteroid dehydrogenase deficiencySex change
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17β-Hydroxysteroid dehydrogenase III deficiency
17β-Hydroxysteroid dehydrogenase III deficiency is a rare autosomal recessive disorder of sexual development, or intersex condition, affecting testosterone biosynthesis by 17β-hydroxysteroid dehydrogenase III (17β-HSD III), which can produce impaired virilization (historically termed male pseudohermaphroditism) of genetically male infants.
has abstract
17β-Hydroxysteroid dehydrogena ...... ) of genetically male infants.
@en
Der Testosteron-17β-Dehydrogen ...... en J. M. Saez und Mitarbeiter.
@de
Дефицит 17β-гидроксистероиддег ...... цев генетически мужского пола.
@ru
DiseasesDB
ICD10
medical diagnosis
OMIM id
symptoms
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Wikipage page ID
10,346,182
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1,019,851,177
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caption
Biochemical effects of 17β-hyd ...... ing to male undervirilization.
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causes
Mutations found in the 17β-HSD III gene
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diagnosis
Genetic testing
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DiseasesDB
ICD
E29.1
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OMIM
Orphanet
symptoms
Hypothyroidism, Cryptorchidism
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synonyms
treatment
Gonads should be monitored
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wikiPageUsesTemplate
subject
comment
17β-Hydroxysteroid dehydrogena ...... ) of genetically male infants.
@en
Der Testosteron-17β-Dehydrogen ...... en J. M. Saez und Mitarbeiter.
@de
Дефицит 17β-гидроксистероиддег ...... цев генетически мужского пола.
@ru
label
17β-Hydroxysteroid dehydrogenase III deficiency
@en
Testosteron-17β-Dehydrogenase-Mangel
@de
Дефицит 17β-гидроксистероиддегидрогеназы III
@ru
isPrimaryTopicOf
name
17β-Hydroxysteroid dehydrogenase III deficiency
@en