Genomics England
GMS Panels
Panels
Genes and Entities
FAM149B1
family with sequence similarity 149 member B1
See this entity in PanelApp
Panel
Mode of inheritance
Details
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in
DDG2P
Component of the following Super Panels:
- Paediatric disorders
Signed-off version 4.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Ciliopathy-related syndromic intellectual disability