Spermatogenic failure 12

Preferred Label : Spermatogenic failure 12;

Symbol : SPGF12;

CISMeF acronym : SPGF12;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the gene encoding homolog of Drosophila NANOS-1 (NANOS1, 608226.0001);

Prefixed ID : #615413;

Details

Origin ID

615413;

UMLS CUI

C3809427;

Currated CISMeF NLP mapping
- spermatogenic failure 12 [DO Concept]
DO Cross reference
- spermatogenic failure 12 [DO Concept]
Genes related to phenotype
- Nanos c2hc-type zinc finger 1 [OMIM gene]
HPO term(s)
- Abnormal male germ cell morphology [HPO term]
- Autosomal dominant inheritance [HPO term]
- Azoospermia [HPO term]
- Infertility [HPO term]
ORDO concept(s)
- Male infertility with azoospermia or oligozoospermia due to single gene mutation [ORDO Disease]
- Male infertility with teratozoospermia due to single gene mutation [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- spermatogenic failure 12 [DO Concept]

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