DCC, DCC netrin 1 receptor, 1630

N. diseases: 279; N. variants: 101
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 CausalMutation disease CLINVAR
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 GeneticVariation disease UNIPROT
CUI: C1834870
Disease: MIRROR MOVEMENTS 1
MIRROR MOVEMENTS 1 		0.700 CausalMutation phenotype CLINVAR
CUI: C1834870
Disease: MIRROR MOVEMENTS 1
MIRROR MOVEMENTS 1 		0.700 Biomarker phenotype GENOMICS_ENGLAND
CUI: C1834870
Disease: MIRROR MOVEMENTS 1
MIRROR MOVEMENTS 1 		0.700 Biomarker phenotype GENOMICS_ENGLAND
CUI: C1834870
Disease: MIRROR MOVEMENTS 1
MIRROR MOVEMENTS 1 		0.700 Biomarker phenotype CTD_human
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		0.510 CausalMutation group CGI
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		0.510 Biomarker group CTD_human
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		0.500 CausalMutation disease CGI
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		0.500 GeneticVariation disease UNIPROT
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus 		0.500 Biomarker disease CTD_human
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus 		0.500 CausalMutation disease CGI
CUI: C4479640
Disease: GAZE PALSY, FAMILIAL HORIZONTAL, WITH PROGRESSIVE SCOLIOSIS, 2
GAZE PALSY, FAMILIAL HORIZONTAL, WITH PROGRESSIVE SCOLIOSIS, 2 		0.500 Biomarker disease GENOMICS_ENGLAND
CUI: C0175754
Disease: Agenesis of corpus callosum
Agenesis of corpus callosum 		0.430 Biomarker disease HPO
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability 		0.410 Biomarker group HPO
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.310 CausalMutation disease CGI
CUI: C0153942
Disease: Benign neoplasm of esophagus
Benign neoplasm of esophagus 		0.300 CausalMutation disease CGI
CUI: C0154059
Disease: Carcinoma in situ of esophagus
Carcinoma in situ of esophagus 		0.300 CausalMutation disease CGI
CUI: C0454455
Disease: Mirror movements disorder
Mirror movements disorder 		0.180 Biomarker disease HPO
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma 		0.130 Biomarker disease HPO
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms 		0.110 Biomarker group HPO
CUI: C4024989
Disease: Hereditary nonpolyposis colorectal carcinoma
Hereditary nonpolyposis colorectal carcinoma 		0.110 Biomarker disease HPO
CUI: C0003126
Disease: Anosmia
Anosmia 		0.100 Biomarker phenotype HPO
CUI: C0004134
Disease: Ataxia
Ataxia 		0.100 Biomarker phenotype HPO
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis 		0.100 Biomarker disease HPO