Genomics England
GMS Panels
Panels
Genes and Entities

ADAMTS10

ADAM metallopeptidase with thrombospondin type 1 motif 10
OMIM: 608990
PanelMode of inheritanceDetails
5 panels
Green
in Arthrogryposis
R-numbers: R83
Signed-off version 6.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Weill-Marchesani syndrome 1, recessive 277600
Green
in Bilateral congenital or childhood onset cataracts
R-numbers: R31
Signed-off version 4.14
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Weill-Marchesani syndrome
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 4.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Weill-Marchesani syndrome 1, recessive 277600
Green
in Skeletal dysplasia
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R104
Signed-off version 5.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Weill-Marchesani syndrome 1, recessive, 277600
Green
in Structural eye disease
R-numbers: R36
Signed-off version 3.79
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Weill-Marchesani syndrome 1, recessive