Cytoscape Web
Click node...

X-linked Emery-Dreifuss muscular dystrophy
2 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Familial primary hypomagnesemia with normocalcuria and normocalcemia
2 OMIM references -
2 associated genes
No signs/symptoms info
X-linked Emery-Dreifuss muscular dystrophy
Familial primary hypomagnesemia with normocalcuria and normocalcemia

EMD
(UniProt - OMIM)
 CNNM2
(UniProt - OMIM)
FHL1
(UniProt - OMIM)
 EGF
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
EMD
(0.63)
EGF


Citations in the biomedical literature:


X-linked Emery-Dreifuss muscular dystrophy
EMD FHL1
Familial primary hypomagnesemia with normocalcuria and normocalcemia
CNNM2 EGF



X-linked Emery-Dreifuss muscular dystrophy
Familial primary hypomagnesemia with normocalcuria and normocalcemia

Synonym(s):
- EDMD1
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
Class of prevalence: unknown
Average age onset: -
Average age of death: -
Type of inheritance: x-linked recessive
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:
2 OMIM references -
No MeSH references
External references:
2 OMIM references -
No MeSH references
No signs/symptoms info available.