ADAMTS19

ADAM metallopeptidase with thrombospondin type 1 motif 19
OMIM: 607513
PanelMode of inheritanceDetails
2 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 7.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
OMIM:620067.0, MONDO:0859572, ADAMTS19-related cardiac valvular dysplasia
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 8.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Non-syndromic heart valve disease, heart valve disease, MONDO:0002869