Spermatogenic failure 52

Summary

Spermatogenic failure-52 (SPGF52) is characterized by azoospermic infertility resulting from meiotic arrest at the spermatocyte stage (Fan et al., 2021). For a discussion of genetic heterogeneity of spermatogenic failure, see SPGF1 (258150). [from OMIM]

Available tests

2 tests are in the database for this condition.

Clinical tests (2 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

Associated genes Help
Genes reported to contribute to the condition.

C14orf39
3 tests
Also known as: POF18, SPGF52, Six6os1, C14orf39
Summary: chromosome 14 open reading frame 39

Imported from Human Phenotype Ontology (HPO)

Show all Hide all

Abnormality of the genitourinary system
- Azoospermia
  Azoospermia
  - MedGen UID: 2150
  - Concept ID: C0004509
  - Finding: Disease or Syndrome
  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

Reviews

Clinical resources

Molecular resources

Consumer resources

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.