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1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
2 OMIM references -
2 associated genes
No signs/symptoms info
Laminopathy type Decaudain-Vigouroux
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:


Laminopathy type Decaudain-Vigouroux
LMNA
Familial primary hypomagnesemia with normocalcuria and normocalcemia
CNNM2 EGF



Laminopathy type Decaudain-Vigouroux
Familial primary hypomagnesemia with normocalcuria and normocalcemia

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

Synonym(s):
(no synonyms)

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

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -

Epidemiological data:
(no data available)
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:
No OMIM references
No MeSH references
External references:
2 OMIM references -
No MeSH references

No signs/symptoms info available.