absent male inguinal canal Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the passage in the lower abdominal wall through which the spermatic cord, nerves and vessels normally pass from the pelvic cavity to the scrotum (Mammalian Phenotype Ontology, MP_0009213)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009213
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Genes

1 gene mutations causing the absent male inguinal canal phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
HOXA10 homeobox A10