Spermatogenic failure 57

Preferred Label : Spermatogenic failure 57;

Symbol : SPGF57;

Type : Phenotype, molecular basis known;

Prefixed ID : #619528;

Origin ID

619528;

UMLS CUI

C5561988;

Genes related to phenotype
- Parn-like ribonuclease domain-containing exonuclease 1 [OMIM gene]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Decreased testicular size [HPO term]
- Male infertility [HPO term]
- Non-obstructive azoospermia [HPO term]
- Spermatogenesis maturation arrest [HPO term]
- Young adult onset [HPO term]
ORDO concept(s)
- Male infertility with azoospermia or oligozoospermia due to single gene mutation [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]