HOXD13

PanelMode of inheritanceDetails
4 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 2.2
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
R-numbers: R21
Signed-off version 1.92
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
SYNPOLYDACTYLY 1, BRACHYDACTYLY TYPE D, BRACHYDACTYLY-SYNDACTYLY SYNDROME, BRACHYDACTYLY TYPE E, VACTERL ASSOCIATION, SYNDACTYLY TYPE 5
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 2.2
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
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R104
Signed-off version 2.2
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