DisGeNET - a database of gene-disease associations

ALDH18A1, aldehyde dehydrogenase 18 family member A1, 5832

N. diseases: 206; N. variants: 22

Disease: Retinal Diseases ×

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:	C0035309
Disease:	Retinal Diseases

Retinal Diseases

0.010

GeneticVariation

group

BEFREE

Cutis laxa, fat pads and retinopathy due to ALDH18A1 mutation and review of the literature.

2014