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1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
4 OMIM references -
3 associated genes
No signs/symptoms info
Laminopathy type Decaudain-Vigouroux
Male infertility with normal virilization due to meiosis defect

LMNA CFTR
SOHLH1
SYCP3


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
LMNA
(0.63)
CFTR



Citations in the biomedical literature:


Laminopathy type Decaudain-Vigouroux
LMNA
Male infertility with normal virilization due to meiosis defect
CFTR SOHLH1 SYCP3



Laminopathy type Decaudain-Vigouroux
Male infertility with normal virilization due to meiosis defect

Synonym(s):
- Laminopathy with severe metabolic syndrome and myopathy

Synonym(s):
- Azoospermia due to maturation arrest
- Azoospermia due to meiosis defect
- Male infertility with normal virilization due to maturation arrest

Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
Classification (Orphanet):
- Rare genetic disease

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
(no data available)

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: adolescence / young
Average age of death: -
Type of inheritance: autosomal dominant

External references:
No OMIM references
No MeSH references
External references:
4 OMIM references -
No MeSH references

No signs/symptoms info available.