ICK

intestinal cell kinase
OMIM: 612325
PanelMode of inheritanceDetails
6 panels
Green
in Clefting
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 6.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Endocrine-cerebroosteodysplasia, OMIM:612651, Endocrine-cerebro-osteodysplasia syndrome, MONDO:0012980
R-numbers: R21, R412
Signed-off version 4.195
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Endocrine-cerebroosteodysplasia, OMIM:612651, Endocrine-cerebro-osteodysplasia syndrome, MONDO:0012980
Component of the following Super Panels:
  • - Hereditary ataxia and cerebellar anomalies - childhood onset
  • - Paediatric disorders
  • - Rare multisystem ciliopathy Super panel
Signed-off version 4.10
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Endocrine-cerebroosteodysplasia, OMIM:612651, Endocrine-cerebro-osteodysplasia syndrome, MONDO:0012980
Component of the following Super Panels:
  • - Cystic renal disease
  • - Paediatric disorders
  • - Rare multisystem ciliopathy Super panel
  • - Unexplained young onset end-stage renal disease
Signed-off version 3.13
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Endocrine-cerebroosteodysplasia, OMIM:612651, Endocrine-cerebro-osteodysplasia syndrome, MONDO:0012980
Component of the following Super Panels:
  • - Paediatric disorders
  • - Rare multisystem ciliopathy Super panel
Signed-off version 5.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Endocrine-cerebroosteodysplasia, OMIM:612651, Endocrine-cerebro-osteodysplasia syndrome, MONDO:0012980
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R104
Signed-off version 6.16
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Endocrine-cerebroosteodysplasia, OMIM:612651, Endocrine-cerebro-osteodysplasia syndrome, MONDO:0012980