DLX5

distal-less homeobox 5
OMIM: 600028
PanelMode of inheritanceDetails
3 panels
R-numbers: R21, R412
Signed-off version 2.1
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
?Split-hand/foot malformation 1 with sensorineural hearing loss, 220600, Split-hand/foot malformation 1, 183600
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 3.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
?Split-hand/foot malformation 1 with sensorineural hearing loss, OMIM:220600, Split-hand/foot malformation 1, OMIM:183600
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R104
Signed-off version 3.1
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
?Split-hand/foot malformation 1 with sensorineural hearing loss, OMIM:220600, Split-hand/foot malformation 1, OMIM:183600