Search Ontology:
Human Disease
17-beta hydroxysteroid dehydrogenase 3 deficiency
- Term ID
- DOID:0112248
- Synonyms
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- 17-beta-hydroxysteroid dehydrogenase 3 deficiency
- 17-ketoreductase deficiency
- 17-ketosteroidreductase deficiency
- 17-KSR deficiency
- 46,XY disorder of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency
- male pseudohermaphroditism with gynecomastia
- neutral 17-beta-hydroxysteroid oxidoreductase deficiency
- Definition
- A pseudohermaphroditism characterized by undermasculinization in males including hypoplastic-to-normal internal genitalia with female external genitalia and the absence of a prostate, impaired testicular synthesis of testosterone resulting in insufficient formation of dihydrotestosterone during fetal development and resulting in pseudohermaphroditism in males that has_material_basis_in homozygous or compound heterozygous mutation of the HSD17B3 gene on chromosome 9q22. (3)
- References
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- GARD:5659
- MIM:264300
- ORDO:752
- Ontology
- Human Disease ( DOID:0112248 )
- is a type of
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Genes Involved
Zebrafish Models