CIT

citron rho-interacting serine/threonine kinase
OMIM: 605629
PanelMode of inheritanceDetails
3 panels
R-numbers: R21, R412
Signed-off version 2.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Microcephaly 17, primary, autosomal recessive, OMIM:617090, Microcephaly 17, primary, autosomal recessive, MONDO:0014908
Component of the following Super Panels:
  • - Hypotonic infant
  • - Paediatric disorders
  • - White matter disorders - childhood onset
R-numbers: R29
Signed-off version 4.4
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Microcephaly 17, primary, autosomal recessive, 617090
R-numbers: R88
Signed-off version 3.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
autosomal-recessive primary microcephaly, MCPH, Microcephaly 17, primary, autosomal recessive, 617090