ADAMTS19

ADAM metallopeptidase with thrombospondin type 1 motif 19
OMIM: 607513, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Green ADAMTS19 in Familial non syndromic congenital heart disease

Level 3: Congenital heart disease
Level 2: Cardiovascular disorders
Version 1.80

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Non-syndromic heart valve disease
  • heart valve disease, MONDO:0002869
Green ADAMTS19 in Paediatric disorders - additional genes


Version 3.9
Latest signed off version: v3.0 (22 Mar 2023)

Component of the following Super Panels:

  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • NHS GMS
    • Expert Review Green
    • Literature
    Phenotypes
    • Non-syndromic heart valve disease
    • heart valve disease, MONDO:0002869