Cytoscape Web
Click node...

Childhood-onset autosomal recessive myopathy with external ophthalmoplegia
1 associated gene
4 connected diseases
No signs/symptoms info
Disease Type of connection
Hereditary inclusion body myopathy - joint contractures - ophthalmoplegia
Juvenile myelomonocytic leukemia
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Adenosine monophosphate deaminase deficiency
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
MYH2 Q9UKX2160740
No signs/symptoms info available.