Spermatogenic failure 87 - CISMeF

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CISMeF

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Spermatogenic failure 87OMIM Phenotype

Preferred Label : Spermatogenic failure 87;

Symbol : SPGF87;

Type : Phenotype, molecular basis known;

Prefixed ID : #620500;

Details

Origin ID

620500;

UMLS CUI

C5882687;

Genes related to phenotype
- Acrosin [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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03/05/2025

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