Vanishing testis


Normal Case/Contol

GWAS of 0012870

Sibling Case/Control

No sibling GWAS available 0012870


Case Control
368 459826

Phenotype Definition

A condition which is considered to be due to the subsequent atrophy and disappearance in fetal life of an initially normal testis. In the presence of spermatic cord structures is evidence of the presence of the testis in early intrauterine life. When associated with a blind-ending spermatic cord, this entity is named as his absence of a testis in an otherwise normal 46XY male is usually unilateral and is assumed to be a consequence of intrauterine or perinatal torsion or infarction. [HPO:probinson, PMID:22985611]

Top SNP Information

Associated Diseases

ID Name Top Correlation
ICD: C629 Testis, unspecified 7/20