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Autosomal dominant centronuclear myopathy
2 OMIM references -
4 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
1 OMIM reference -
1 associated gene
No signs/symptoms info
Autosomal dominant centronuclear myopathy
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

DNM2
(UniProt - OMIM)
 APP
(UniProt - OMIM)
MTMR14
(UniProt - OMIM)
MYF6
(UniProt - OMIM)
RYR1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
DNM2
MTMR14
(0.56)
(0.56)
APP
APP


Citations in the biomedical literature:


Autosomal dominant centronuclear myopathy
DNM2 MTMR14 MYF6 RYR1
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP



Autosomal dominant centronuclear myopathy
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

Synonym(s):
- AD-CNM
Synonym(s):
- HCHWA, Flemish type
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: adolescence / young
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
2 OMIM references -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.