Genomics England
GMS Panels
Panels
Genes and Entities

HOXD13

homeobox D13
OMIM: 142989
PanelMode of inheritanceDetails
4 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 4.15
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
BRACHYDACTYLY-SYNDACTYLY SYNDROME 610713, VACTERL ASSOCIATION 192350, BRACHYDACTYLY TYPE E 113300, SYNPOLYDACTYLY 1 186000, SYNDACTYLY TYPE 5 186300, BRACHYDACTYLY TYPE D 113200
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 4.195
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
SYNPOLYDACTYLY 1, BRACHYDACTYLY TYPE D, BRACHYDACTYLY-SYNDACTYLY SYNDROME, BRACHYDACTYLY TYPE E, VACTERL ASSOCIATION, SYNDACTYLY TYPE 5
Green
in Limb disorders
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 6.2
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Brachydactyly-syndactyly syndrome 610713, Brachydactyly, type D 113200, Brachydactyly, type E 113300, Syndactyly, type V 186300, Synpolydactyly 1 186000, Polydactyly
Green
in Skeletal dysplasia
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R104
Signed-off version 6.16
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Syndactyly, type V 186300, Brachydactyly-syndactyly syndrome 610713, Brachydactyly, type E 113300, Synpolydactyly 1 186000, Brachydactyly, type D 113200