DisGeNET - a database of gene-disease associations

LDB3, LIM domain binding 3, 11155

N. diseases: 69; N. variants: 15

Disease: MYOPATHY, MYOFIBRILLAR, 4 ×

Source: ALL

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

Disease

Score _gda

Association Type

Type

Original DB

Sentence supporting the association

PMID

PMID Year

CUI:	C4721886
Disease:	MYOPATHY, MYOFIBRILLAR, 4

MYOPATHY, MYOFIBRILLAR, 4

0.400

Biomarker

disease

GENOMICS_ENGLAND

Mutations in ZASP define a novel form of muscular dystrophy in humans.

15668942

2005

CUI:	C4721886
Disease:	MYOPATHY, MYOFIBRILLAR, 4

MYOPATHY, MYOFIBRILLAR, 4

0.400

Biomarker

disease

GENOMICS_ENGLAND

Mutations in ZASP define a novel form of muscular dystrophy in humans.

15668942

2005

CUI:	C4721886
Disease:	MYOPATHY, MYOFIBRILLAR, 4

MYOPATHY, MYOFIBRILLAR, 4

0.400

Biomarker

disease

GENOMICS_ENGLAND

CUI:	C4721886
Disease:	MYOPATHY, MYOFIBRILLAR, 4

MYOPATHY, MYOFIBRILLAR, 4

0.400

CausalMutation

disease

CLINVAR