Spermatogenic failure 69

Summary

Spermatogenic failure-69 (SPGF69) is characterized by male infertility due to sperm being round-headed (globozoospermia) and lacking the acrosome (Oud et al., 2020). For a general phenotypic description and discussion of genetic heterogeneity of spermatogenic failure, see SPGF1 (258150). [from OMIM]

Genes See tests for all associated and related genes

Associated genes Help
Genes reported to contribute to the condition.

GGN
Also known as: , GGN
Summary: gametogenetin

Imported from Human Phenotype Ontology (HPO)

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Abnormality of the genitourinary system
- Globozoospermia
  Globozoospermia
  - MedGen UID: 96048
  - Concept ID: C0403825
  - Finding: Finding
  Abnormality of the genitourinary system
  See: Feature record | Search on this feature
- Male infertility
  Male infertility
  - MedGen UID: 5796
  - Concept ID: C0021364
  - Finding: Disease or Syndrome
  Abnormality of the genitourinary system
  See: Feature record | Search on this feature

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