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1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
5 OMIM references -
5 associated genes
No signs/symptoms info
Laminopathy type Decaudain-Vigouroux
Congenital muscular dystrophy with intellectual disability

LMNA FKRP
GMPPB
LARGE
POMT1
POMT2


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Laminopathy type Decaudain-Vigouroux
LMNA
Congenital muscular dystrophy with intellectual disability
FKRP GMPPB LARGE POMT1 POMT2



Laminopathy type Decaudain-Vigouroux
Congenital muscular dystrophy with intellectual disability

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

Synonym(s):
- CMD with intellectual disability
- CMD-MR

Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
(no data available)
Epidemiological data:
(no data available)

External references:
No OMIM references
No MeSH references
External references:
5 OMIM references -
No MeSH references

No signs/symptoms info available.