Spermatogenic failure 21

Preferred Label : Spermatogenic failure 21;

Symbol : SPGF21;

CISMeF acronym : SPGF21;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal recessive;

Molecular basis : Caused by mutation in the testis-specific bromodomain gene (BRDT, 602144.0001);

Prefixed ID : #617644;

Details

Origin ID

617644;

UMLS CUI

C4539991;

Currated CISMeF NLP mapping
- spermatogenic failure 21 [DO Concept]
DO Cross reference
- spermatogenic failure 21 [DO Concept]
Genes related to phenotype
- Bromodomain, testis-specific [OMIM gene]
HPO term(s)
- Acephalic spermatozoa [HPO term]
- Autosomal recessive inheritance [HPO term]
- Infertility [HPO term]
- Reduced sperm motility [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- spermatogenic failure 21 [DO Concept]

Keyword's position in hierarchy(ies) :

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