Genomics England
GMS Panels
Panels
Genes and Entities

ALX4

ALX homeobox 4
OMIM: 605420
PanelMode of inheritanceDetails
4 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 4.15
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
PARIETAL FORAMINA 2 609597, FRONTONASAL DYSPLASIA 2 613451
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 4.195
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
FRONTONASAL DYSPLASIA 2, PARIETAL FORAMINA 2
Green
in Rare syndromic craniosynostosis or isolated multisuture synostosis
R-numbers: R100
Signed-off version 5.0
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Parietal foramina, Parietal foramina 2, (AD), 609597, Frontonasal dysplasia 2, (AR), 613451
Green
in Skeletal dysplasia
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R104
Signed-off version 6.16
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Frontonasal dysplasia 2 613451