Genomics England
GMS Panels
Panels
Genes and Entities
DTNA
dystrobrevin alpha
OMIM:
601239
See this entity in PanelApp
Panel
Mode of inheritance
Details
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Congenital muscular dystrophy and congenital myopathy
Component of the following Super Panels:
- Hypotonic infant
- Other rare neuromuscular disorders
R-numbers:
R432
Signed-off version 1.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
muscular dystrophy, MONDO:0020121