DisGeNET - a database of gene-disease associations

Source: ORPHANET

Disease: Retinitis Pigmentosa ×

Gene: CDHR1 ×

Results per page

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

Gene

Disease

Score _gda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

Entrez Id:	92211
Gene Symbol:	CDHR1

CDHR1

CUI:	C0035334
Disease:	Retinitis Pigmentosa

Retinitis Pigmentosa

0.400

GermlineCausalMutation

ORPHANET

Biallelic mutation of protocadherin-21 (PCDH21) causes retinal degeneration in humans.

2010