Spermatogenic failure 51

Preferred Label : Spermatogenic failure 51;

Symbol : SPGF51;

Type : Phenotype, molecular basis known;

Prefixed ID : #619177;

Origin ID

619177;

UMLS CUI

C5543033;

Genes related to phenotype
- Cilia- and flagella-associated protein 91 [OMIM gene]
HPO term(s)
- Absent sperm axoneme central pair complex [HPO term]
- Absent sperm flagella [HPO term]
- Autosomal recessive inheritance [HPO term]
- Coiled sperm flagella [HPO term]
- Irregularly shaped sperm tail [HPO term]
- Macrocephalic sperm head [HPO term]
- Microcephalic sperm head [HPO term]
- Oligospermia [HPO term]
- Reduced sperm motility [HPO term]
- Short sperm flagella [HPO term]
ORDO concept(s)
- Male infertility with teratozoospermia due to single gene mutation [ORDO Disease]
See also inter- (CISMeF)
- Male infertility with teratozoospermia due to single gene mutation [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]