DCC, DCC netrin 1 receptor, 1630

N. diseases: 279; N. variants: 101
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C0017570
Disease: Gingival Neoplasms
Gingival Neoplasms 		group Neoplasms; Stomatognathic Diseases Neoplastic Process 1 0.010 None 1.000 1 2002 2002
CUI: C4479640
Disease: GAZE PALSY, FAMILIAL HORIZONTAL, WITH PROGRESSIVE SCOLIOSIS, 2
GAZE PALSY, FAMILIAL HORIZONTAL, WITH PROGRESSIVE SCOLIOSIS, 2 		disease Disease or Syndrome 1 1 0.500 None 1.000 1 1 2017 2017
CUI: C4015970
Disease: ESOPHAGEAL CARCINOMA, SOMATIC
ESOPHAGEAL CARCINOMA, SOMATIC 		disease Neoplastic Process 1 1 0.100 None 0 1
CUI: C1834870
Disease: MIRROR MOVEMENTS 1
MIRROR MOVEMENTS 1 		phenotype Finding 2 11 0.700 limited 1.000 2 11 2010 2017
CUI: C3179058
Disease: Corpus Callosum Malformation
Corpus Callosum Malformation 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Congenital Abnormality 2 0.300 None 1.000 1 2017 2017
CUI: C0429702
Disease: Respiratory quotient
Respiratory quotient 		phenotype Clinical Attribute 3 3 0.100 None 1.000 1 1 2012 2012
CUI: C1846496
Disease: Gaze Palsy, Familial Horizontal, with Progressive Scoliosis
Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 		disease Musculoskeletal Diseases Disease or Syndrome 3 0.300 None 1.000 1 2017 2017
CUI: C4024794
Disease: Horizontal supranuclear gaze palsy
Horizontal supranuclear gaze palsy 		disease Disease or Syndrome 3 1 0.100 None 1.000 1 1 2017 2017
CUI: C4551964
Disease: GAZE PALSY, FAMILIAL HORIZONTAL, WITH PROGRESSIVE SCOLIOSIS, 1
GAZE PALSY, FAMILIAL HORIZONTAL, WITH PROGRESSIVE SCOLIOSIS, 1 		disease Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Eye Diseases; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 3 11 0.300 None 1.000 1 2017 2017
CUI: C4025704
Disease: Abnormality of the corticospinal tract
Abnormality of the corticospinal tract 		phenotype Anatomical Abnormality 5 0.100 None 0
CUI: C4476591
Disease: Dysgenesis of the hippocampus
Dysgenesis of the hippocampus 		disease Congenital Abnormality 5 0.100 None 0
CUI: C0153942
Disease: Benign neoplasm of esophagus
Benign neoplasm of esophagus 		disease Digestive System Diseases; Neoplasms Neoplastic Process 6 0.300 None 0
CUI: C0154059
Disease: Carcinoma in situ of esophagus
Carcinoma in situ of esophagus 		disease Digestive System Diseases; Neoplasms Neoplastic Process 6 0.300 None 0
CUI: C0242287
Disease: Isaacs syndrome
Isaacs syndrome 		disease Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 13 9 0.010 None 1.000 1 2017 2017
CUI: C3887527
Disease: Fused cervical vertebrae
Fused cervical vertebrae 		disease Congenital Abnormality 15 2 0.100 None 0
CUI: C1858361
Disease: Pyogenic Arthritis, Pyoderma Gangrenosum and Acne
Pyogenic Arthritis, Pyoderma Gangrenosum and Acne 		disease Infections; Skin and Connective Tissue Diseases; Musculoskeletal Diseases Disease or Syndrome 21 7 0.010 None 1.000 1 2018 2018
CUI: C4025644
Disease: Hypothalamic gonadotropin-releasing hormone deficiency
Hypothalamic gonadotropin-releasing hormone deficiency 		phenotype Finding 22 0.100 None 0
CUI: C3898222
Disease: mucosal melanoma
mucosal melanoma 		disease Neoplastic Process 24 1 0.010 None 1.000 1 2018 2018
CUI: C4022003
Disease: Erectile abnormalities
Erectile abnormalities 		disease Finding 24 0.100 None 0
CUI: C4745063
Disease: Biliary Tract Carcinoma
Biliary Tract Carcinoma 		disease Neoplastic Process 25 1 0.010 None 1.000 1 2019 2019
CUI: C3899403
Disease: Decreased Concentration
Decreased Concentration 		phenotype Sign or Symptom 27 1 0.010 None 1.000 1 2011 2011
CUI: C4024989
Disease: Hereditary nonpolyposis colorectal carcinoma
Hereditary nonpolyposis colorectal carcinoma 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Nutritional and Metabolic Diseases Neoplastic Process 28 5 0.110 None 1.000 1 1991 1991
CUI: C1867864
Disease: Poor fine motor coordination
Poor fine motor coordination 		phenotype Finding 31 3 0.100 None 0
CUI: C0027814
Disease: Neuritis, Autoimmune, Experimental
Neuritis, Autoimmune, Experimental 		disease Immune System Diseases; Nervous System Diseases Experimental Model of Disease 32 0.200 None 1.000 1 2006 2006
CUI: C3146252
Disease: Stage II Colorectal Cancer AJCC v7
Stage II Colorectal Cancer AJCC v7 		disease Neoplastic Process 32 0.010 None 1.000 1 1998 1998