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References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 22/06/2006 |
Symbol | CPTD |
Location | 13q12.1 |
Name | cryptorchidism, unilateral or bilateral |
Other name(s) |
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Corresponding gene | RXFP2 |
Main clinical features | failure of testitular descent, with infertility, increased risk of testicular malignancy |
Genetic determination | autosomal recessive |
Function/system disorder | sex-genitalia |
Type | disease |
Gene product |
Name | G protein coupled receptor affecting testicular descent |
Remark(s) |