Spermatogenic failure 73

Preferred Label : Spermatogenic failure 73;

Symbol : SPGF73;

Type : Phenotype, molecular basis known;

Prefixed ID : #619878;

Origin ID

619878;

UMLS CUI

C5676988;

Currated CISMeF NLP mapping
- spermatogenic failure 73 [DO Concept]
DO Cross reference
- spermatogenic failure 73 [DO Concept]
Genes related to phenotype
- Mov10-like risc complex rna helicase 1 [OMIM gene]
HPO term(s)
- Autosomal recessive inheritance [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]
See also inter- (CISMeF)
- Male infertility with azoospermia or oligozoospermia due to single gene mutation [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]