Genomics England
GMS Panels
Panels
Genes and Entities
AFF3
AF4/FMR2 family member 3
OMIM:
601464
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Panel
Mode of inheritance
Details
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in
Genetic epilepsy syndromes
R-numbers:
R59
Signed-off version 3.1
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Intellectual disability, Seizures, KINSSHIP syndrome