DisGeNET - a database of gene-disease associations

Source: LHGDN

Disease: Lecithin Acyltransferase Deficiency ×

Gene: LCAT ×

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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:	3931
Gene Symbol:	LCAT

LCAT

CUI:	C0023195
Disease:	Lecithin Acyltransferase Deficiency

Lecithin Acyltransferase Deficiency

1.000

Biomarker

LHGDN

[Fish eye disease revealing a partial LCAT deficiency].

2005