Genomics England
GMS Panels
Panels
Genes and Entities

CCDC88A

coiled-coil domain containing 88A
OMIM: 609736
PanelMode of inheritanceDetails
4 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 5.48
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
PEHO-like syndrome
Green
in Early onset or syndromic epilepsy
Component of the following Super Panels:
  • - Paediatric disorders
  • - Unexplained death in infancy and sudden unexplained death in childhood
R-numbers: R59
Signed-off version 7.54
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
PEHO syndrome-like, OMIM:617507
Green
in Intellectual disability
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 8.134
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
PEHO syndrome-like, OMIM:617507
Green
in Severe microcephaly
R-numbers: R88
Signed-off version 7.16
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
PEHO syndrome-like, OMIM:617507