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References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 29-01-2009 |
Symbol | CRD2 |
Location | 1p36.22 |
Name | cortisone reductase deficiency 2 |
Corresponding gene | H6PD |
Main clinical features |
|
Genetic determination | autosomal recessive |
Function/system disorder | endocrinology |
Type | disease |
Remark(s) |