Genomics England
GMS Panels
Panels
Genes and Entities
INO80
INO80 complex subunit
OMIM:
610169
See this entity in PanelApp
Panel
Mode of inheritance
Details
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Primary immunodeficiency or monogenic inflammatory bowel disease
R-numbers:
R15
Signed-off version 6.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
INO80 deficiency, HIGM, severe bacterial infections, Severe bacterial infections, Predominantly Antibody Deficiencies