ICK

intestinal cell kinase
OMIM: 612325
PanelMode of inheritanceDetails
7 panels
Green
in Clefting
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 3.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Endocrine-cerebroosteodysplasia, OMIM:612651, Endocrine-cerebro-osteodysplasia syndrome, MONDO:0012980
R-numbers: R21, R412
Signed-off version 2.4
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 2.1
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
Signed-off version 2.2
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 2.2
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 3.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Endocrine-cerebroosteodysplasia, OMIM:612651, Endocrine-cerebro-osteodysplasia syndrome, MONDO:0012980
R-numbers: R257
Signed-off version 2.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Endocrine-cerebroosteodysplasia, OMIM:612651, Endocrine-cerebro-osteodysplasia syndrome, MONDO:0012980