DisGeNET - a database of gene-disease associations

Gene: RDH10 ×

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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

Gene

Disease

Score _gda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

Entrez Id:	157506
Gene Symbol:	RDH10

RDH10

CUI:	C0376634
Disease:	Craniofacial Abnormalities

Craniofacial Abnormalities

0.300

Biomarker

CTD_human

Characterization of human short chain dehydrogenase/reductase SDR16C family members related to retinol dehydrogenase 10.

2017