DisGeNET - a database of gene-disease associations

ADAMTS10, ADAM metallopeptidase with thrombospondin type 1 motif 10, 81794

N. diseases: 67; N. variants: 12

Disease: Microspherophakia ×

Source: ALL

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Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _g

DPI _g

pLI

EI _gda

EL _gda

Score _gda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Disease

Score _gda

Association Type

Type

Original DB

Sentence supporting the association

PMID

PMID Year

CUI:	C1562061
Disease:	Microspherophakia

Microspherophakia

0.110

GeneticVariation

disease

BEFREE

Our study suggests that isolated microspherophakia and the Weill-Marchesani Syndrome are not allelic to the ADAMTS10 gene.

19696795

2009

CUI:	C1562061
Disease:	Microspherophakia

Microspherophakia

0.110

Biomarker

disease

HPO