ADAMTS10

ADAM metallopeptidase with thrombospondin type 1 motif 10
OMIM: 608990, ClinGen, DECIPHER

10 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 10 panels
Green ADAMTS10 in Aortopathy_Connective Tissue Disorders Level 2: Cardiovascular disorders Version 2.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Other Phenotypes Weill-Marchesani syndrome 1, recessive MIM#277600
Green ADAMTS10 in Arthrogryposis Level 2: Neurology and neurodevelopmental disorders Version 2.0	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert list Victorian Clinical Genetics Services Phenotypes Weill-Marchesani syndrome 1, recessive, MIM#277600
Green ADAMTS10 in Cataract Level 2: Ophthalmological disorders Version 1.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert list Victorian Clinical Genetics Services Victorian Clinical Genetics Services Phenotypes Weill-Marchesani syndrome 1, recessive, MIM#277600
Green ADAMTS10 in Congenital Heart Defect Level 2: Cardiovascular disorders Version 1.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Weill-Marchesani syndrome 1, recessive, MIM# 277600
Green ADAMTS10 in Glaucoma congenital Level 2: Ophthalmological disorders Version 2.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert list Phenotypes Weill-Marchesani syndrome 1, recessive, MIM# 277600
Green ADAMTS10 in Mendeliome Version 2.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert list Victorian Clinical Genetics Services Phenotypes Weill-Marchesani syndrome 1, recessive, MIM#277600
Green ADAMTS10 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 2.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Genetic Health Queensland Phenotypes Weill-Marchesani syndrome 1, recessive, MIM#277600
Green ADAMTS10 in Skeletal dysplasia Level 3: Skeletal dysplasias Level 2: Skeletal disorders Version 1.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green NHS GMS Expert list Victorian Clinical Genetics Services Phenotypes Weill-Marchesani syndrome 1, recessive, 277600
Green ADAMTS10 in Hand and foot malformations Level 2: Dysmorphic and congenital abnormality syndromes Version 1.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert list Expert Review Green Expert Review Green Expert list Victorian Clinical Genetics Services Expert Review Green Phenotypes Weill-Marchesani syndrome 1, recessive, 277600
Green ADAMTS10 in Fetal anomalies Version 2.0	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Genomics England PanelApp Genetic Health Queensland Phenotypes Weill-Marchesani syndrome 1, recessive, MIM#277600