STRADA

STE20-related kinase adaptor alpha
OMIM: 608626
PanelMode of inheritanceDetails
5 panels
R-numbers: R21, R412
Signed-off version 2.4
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Polyhydramnios, megalencephaly, and symptomatic epilepsy, OMIM:611087, Polyhydramnios, megalencephaly, and symptomatic epilepsy, MONDO:0012611
R-numbers: R59
Signed-off version 3.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Polyhydramnios, megalencephaly, and symptomatic epilepsy 611087
Green
in Hydrocephalus
R-numbers: R86
Signed-off version 3.5
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Polyhydramnios, megalencephaly, and symptomatic epilepsy, OMIM:611087
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
Polyhydramnios, megalencephaly, and symptomatic epilepsy, MIM:611087 (includes mental retardation), severe psychomotor retardation
R-numbers: R256
Signed-off version 3.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Polyhydramnios, megalencephaly, and symptomatic epilepsy, 611087