Spermatogenic failure 73 - CISMeF

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CISMeF

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Spermatogenic failure 73OMIM Phenotype

Preferred Label : Spermatogenic failure 73;

Symbol : SPGF73;

Type : Phenotype, molecular basis known;

Prefixed ID : #619878;

Details

Origin ID

619878;

UMLS CUI

C5676988;

Genes related to phenotype
- Mov10-like risc complex rna helicase 1 [OMIM gene]
ORDO concept(s)
- Male infertility with azoospermia or oligozoospermia due to single gene mutation [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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06/05/2025

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