Spermatogenic failure 26

Preferred Label : Spermatogenic failure 26;

Symbol : SPGF26;

CISMeF acronym : SPGF26;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal recessive;

Molecular basis : Caused by mutation in the testis-specific protein 10 gene (TSGA10, 607166.0001);

Prefixed ID : #617961;

Details

Origin ID

617961;

UMLS CUI

C4693773;

Automatic exact mappings (from CISMeF team)
- spermatogenic failure 26 [DO Concept]
DO Cross reference
- spermatogenic failure 26 [DO Concept]
Genes related to phenotype
- Testis-specific protein 10 [OMIM gene]
HPO term(s)
- Acephalic spermatozoa [HPO term]
- Autosomal recessive inheritance [HPO term]
- Infertility [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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