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1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
5 OMIM references -
3 associated genes
No signs/symptoms info
Laminopathy type Decaudain-Vigouroux
Periventricular nodular heterotopia

LMNA ARFGEF2
ERMARD
FLNA


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
LMNA
(0.73)
FLNA



Citations in the biomedical literature:


Laminopathy type Decaudain-Vigouroux
LMNA
Periventricular nodular heterotopia
ARFGEF2 ERMARD FLNA



Laminopathy type Decaudain-Vigouroux
Periventricular nodular heterotopia

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 genetic disease
- Rare neurologic 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: unknown
Average age onset: -
Average age of death: -
Type of inheritance: autosomal recessive

External references:
No OMIM references
No MeSH references
External references:
5 OMIM references -
1 MeSH reference: D054091

No signs/symptoms info available.