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1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
13 OMIM references -
10 associated genes
No signs/symptoms info
Laminopathy type Decaudain-Vigouroux
Nuclear cataract

LMNA CRYAA
CRYBB1
CRYBB2
CRYBB3
CRYGD
FYCO1
GJA3
MIP
NHS
WFS1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
LMNA
(0.72)
FYCO1



Citations in the biomedical literature:


Laminopathy type Decaudain-Vigouroux
LMNA
Nuclear cataract
CRYAA CRYBB1 CRYBB2 CRYBB3 CRYGD FYCO1
GJA3 MIP NHS WFS1



Laminopathy type Decaudain-Vigouroux
Nuclear cataract

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

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

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

External references:
No OMIM references
No MeSH references
External references:
13 OMIM references -
No MeSH references

No signs/symptoms info available.