Spermatogenic failure 47

Preferred Label : Spermatogenic failure 47;

Symbol : SPGF47;

Type : Phenotype, molecular basis known;

Prefixed ID : #619102;

Origin ID

619102;

UMLS CUI

C5436818;

Currated CISMeF NLP mapping
- spermatogenic failure 47 [DO Concept]
DO Cross reference
- spermatogenic failure 47 [DO Concept]
Genes related to phenotype
- Daz-interacting zinc finger protein 1 [OMIM gene]
HPO term(s)
- Absent sperm flagella [HPO term]
- Autosomal recessive inheritance [HPO term]
- Immotile sperm [HPO term]
- Male infertility [HPO term]
- Oligospermia [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]