Genomics England
GMS Panels
Panels
Genes and Entities

ALX1

ALX homeobox 1
OMIM: 601527
PanelMode of inheritanceDetails
5 panels
Green
in Clefting
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 6.5
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Frontonasal dysplasia 3, OMIM:613456, frontonasal dysplasia - severe microphthalmia - severe facial clefting syndrome, MONDO:0013271
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 6.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
FRONTONASAL DYSPLASIA TYPE 3 136760
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 6.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
FRONTONASAL DYSPLASIA TYPE 3
Green
in Skeletal dysplasia
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R104
Signed-off version 8.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Frontonasal dysplasia type 3 613456, Frontonasal dysplasia 3 613456
Green
in Structural eye disease
R-numbers: R36
Signed-off version 4.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Frontonasal dysplasia 3, OMIM:613456, frontonasal dysplasia - severe microphthalmia - severe facial clefting syndrome, MONDO:0013271