Disease #01628 (3 beta-hydroxysteroid dehydrogenase deficiency, OMIM:201810)
Official abbreviation |
- |
Name |
3 beta-hydroxysteroid dehydrogenase deficiency |
OMIM ID |
201810 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
HSD3B2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
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