CDK5RAP2

CDK5 regulatory subunit associated protein 2
OMIM: 608201
PanelMode of inheritanceDetails
3 panels
R-numbers: R21, R412
Signed-off version 2.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Microcephaly 3, primary, autosomal recessive, OMIM:604804, Microcephaly 3, primary, autosomal recessive, MONDO:0011488
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 3, primary, autosomal recessive, 604804, PRIMARY AUTOSOMAL RECESSIVE MICROCEPHALY
R-numbers: R88
Signed-off version 3.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
MCPH, primary microcephaly, Primary Microcephaly, Recessive, Microcephaly 3, primary, autosomal recessive, 604804, Microcephaly 3, Primary, Autosomal Recessive