spermatogenic failure 7

Preferred Label : spermatogenic failure 7;

MeSH note : associated with mutations in CATSPER1;

MeSH synonym : male infertility, nonsyndromic, autosomal recessive;

Details

Origin ID

C567832;

UMLS CUI

C2751811;

Currated CISMeF NLP mapping
- Spermatogenic failure 7 [OMIM Phenotype]
- spermatogenic failure 7 [DO Concept]
DO Cross reference
- spermatogenic failure 7 [DO Concept]
MeSH term(s) associated for indexing
- asthenozoospermia [MeSH Descriptor]
Record concept(s)
- spermatogenic failure 7 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Spermatogenic failure 7 [OMIM Phenotype]
- spermatogenic failure 7 [DO Concept]

Keyword's position in hierarchy(ies) :

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