DisGeNET - a database of gene-disease associations

CDON, cell adhesion associated, oncogene regulated, 50937

N. diseases: 80; N. variants: 10

Source: ALL

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _v

DPI _v

pLI

EI _vda

EL _gda

Score _vda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Variant

Gene

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs369673018

Entrez Id:	50937
Gene Symbol:	CDON

CDON

CUI:	C3280215
Disease:

HOLOPROSENCEPHALY 11

0.800

GeneticVariation

UNIPROT

Mutations in CDON, encoding a hedgehog receptor, result in holoprosencephaly and defective interactions with other hedgehog receptors.

21802063

2011

dbSNP:

rs387906995

Entrez Id:	50937
Gene Symbol:	CDON

CDON

CUI:	C3280215
Disease:

HOLOPROSENCEPHALY 11

0.800

GeneticVariation

UNIPROT

Mutations in CDON, encoding a hedgehog receptor, result in holoprosencephaly and defective interactions with other hedgehog receptors.

21802063

2011

dbSNP:

rs387906996

Entrez Id:	50937
Gene Symbol:	CDON

CDON

CUI:	C3280215
Disease:

HOLOPROSENCEPHALY 11

0.800

GeneticVariation

UNIPROT

Mutations in CDON, encoding a hedgehog receptor, result in holoprosencephaly and defective interactions with other hedgehog receptors.

21802063

2011

dbSNP:

rs387906997

Entrez Id:	50937
Gene Symbol:	CDON

CDON

CUI:	C3280215
Disease:

HOLOPROSENCEPHALY 11

0.800

GeneticVariation

UNIPROT

Mutations in CDON, encoding a hedgehog receptor, result in holoprosencephaly and defective interactions with other hedgehog receptors.

21802063

2011

dbSNP:

rs369673018

Entrez Id:	50937
Gene Symbol:	CDON

CDON

CUI:	C3280215
Disease:

HOLOPROSENCEPHALY 11

0.800

CausalMutation

CLINVAR

dbSNP:

rs387906995

Entrez Id:	50937
Gene Symbol:	CDON

CDON

CUI:	C3280215
Disease:

HOLOPROSENCEPHALY 11

0.800

CausalMutation

CLINVAR

dbSNP:

rs387906996

Entrez Id:	50937
Gene Symbol:	CDON

CDON

CUI:	C3280215
Disease:

HOLOPROSENCEPHALY 11

0.800

CausalMutation

CLINVAR

dbSNP:

rs387906997

Entrez Id:	50937
Gene Symbol:	CDON

CDON

CUI:	C3280215
Disease:

HOLOPROSENCEPHALY 11

0.800

CausalMutation

CLINVAR

dbSNP:

rs183951714

Entrez Id:	50937
Gene Symbol:	CDON

CDON

CUI:	C0022661
Disease:

Kidney Failure, Chronic

0.700

GeneticVariation

GWASCAT

Genetics of Chronic Kidney Disease Stages Across Ancestries: The PAGE Study.

31178898

2019

dbSNP:

rs562022020

Entrez Id:	50937
Gene Symbol:	CDON

CDON

CUI:	C2985280
Disease:

Blood Protein Measurement

0.700

GeneticVariation

GWASCAT

Genomic atlas of the human plasma proteome.

29875488

2018

dbSNP:

rs60929339

Entrez Id:	50937
Gene Symbol:	CDON

CDON

CUI:	C2985280
Disease:

Blood Protein Measurement

0.700

GeneticVariation

GWASCAT

Co-regulatory networks of human serum proteins link genetics to disease.

30072576

2018

dbSNP:

rs139323558

Entrez Id:	50937
Gene Symbol:	CDON

CDON

CUI:	C3280215
Disease:

HOLOPROSENCEPHALY 11

0.700

GeneticVariation

UNIPROT

Mutations in CDON, encoding a hedgehog receptor, result in holoprosencephaly and defective interactions with other hedgehog receptors.

21802063

2011

dbSNP:

rs145983470

Entrez Id:	50937
Gene Symbol:	CDON

CDON

CUI:	C3280215
Disease:

HOLOPROSENCEPHALY 11

0.700

GeneticVariation

UNIPROT

dbSNP:

rs754025360

Entrez Id:	50937
Gene Symbol:	CDON

CDON

CUI:	C4021085
Disease:

Abnormality of brain morphology

0.700

GeneticVariation

CLINVAR