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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
2 OMIM references -
2 associated genes
No signs/symptoms info
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Familial primary hypomagnesemia with normocalcuria and normocalcemia

LMNA CNNM2
EGF


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
LMNA
(0.67)
EGF



Citations in the biomedical literature:


Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
LMNA
Familial primary hypomagnesemia with normocalcuria and normocalcemia
CNNM2 EGF



Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Familial primary hypomagnesemia with normocalcuria and normocalcemia

Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare renal disease

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

Epidemiological data:
Class of prevalence: unknown
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: any age
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
No MeSH references
External references:
2 OMIM references -
No MeSH references

No signs/symptoms info available.