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Amish nemaline myopathy
1 associated gene
12 connected diseases
No signs/symptoms info
Disease Type of connection
Familial isolated dilated cardiomyopathy
Familial thoracic aortic aneurysm and aortic dissection
Left ventricular noncompaction
Digitotalar dysmorphism
Sheldon-Hall syndrome
Acute infantile liver failure-multisystemic involvement syndrome
Pulverulent cataract
Brachydactyly type A2
Brachydactyly type C
Familial isolated restrictive cardiomyopathy
Loeys-Dietz syndrome type 1
Multiple keratoacanthoma, Ferguson-Smith type
Synonym(s):
(no synonyms)
Classification (Orphanet):
- 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: neonatal/infancy
Average age of death: before age 5
Type of inheritance: autosomal recessive
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
TNNT1 P13805191041
No signs/symptoms info available.