DisGeNET - a database of gene-disease associations

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:	C0036439
Disease:	Scoliosis, unspecified

Scoliosis, unspecified

0.010

GeneticVariation

disease

LHGDN

Allelic variants of human melatonin 1A receptor in patients with familial adolescent idiopathic scoliosis.

2003