NTN1, netrin 1, 9423

N. diseases: 209; N. variants: 16
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: C4748869
Disease: MIRROR MOVEMENTS 4
MIRROR MOVEMENTS 4 		disease Disease or Syndrome 1 3 0.400 None 1.000 1 3 2017 2017
CUI: C3275929
Disease: Superior semicircular canal dehiscence syndrome
Superior semicircular canal dehiscence syndrome 		disease Otorhinolaryngologic Diseases Disease or Syndrome 3 0.010 None 1.000 1 2012 2012
CUI: C3854373
Disease: Morvan syndrome
Morvan syndrome 		disease Nervous System Diseases Disease or Syndrome 4 0.020 None 0.500 2 2017 2017
CUI: C1868702
Disease: Diabetic keratopathy
Diabetic keratopathy 		disease Disease or Syndrome 5 0.010 None 1.000 1 2018 2018
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: C0270192
Disease: Perinatal Subarachnoid Hemorrhage
Perinatal Subarachnoid Hemorrhage 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Pathologic Function 8 0.300 None 1.000 1 2018 2018
CUI: C0472383
Disease: Subarachnoid Hemorrhage, Spontaneous
Subarachnoid Hemorrhage, Spontaneous 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Pathologic Function 8 0.300 None 1.000 1 2018 2018
CUI: C0472387
Disease: Vasogenic Cerebral Edema
Vasogenic Cerebral Edema 		phenotype Nervous System Diseases Pathologic Function 8 0.300 None 1.000 1 2018 2018
CUI: C0472388
Disease: Cytotoxic Cerebral Edema
Cytotoxic Cerebral Edema 		phenotype Nervous System Diseases Pathologic Function 8 0.300 None 1.000 1 2018 2018
CUI: C0750969
Disease: Vasogenic Brain Edema
Vasogenic Brain Edema 		phenotype Nervous System Diseases Pathologic Function 8 0.300 None 1.000 1 2018 2018
CUI: C0750970
Disease: Cytotoxic Brain Edema
Cytotoxic Brain Edema 		phenotype Nervous System Diseases Pathologic Function 8 0.300 None 1.000 1 2018 2018
CUI: C0751530
Disease: Subarachnoid Hemorrhage, Aneurysmal
Subarachnoid Hemorrhage, Aneurysmal 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Pathologic Function 8 0.300 None 1.000 1 2018 2018
CUI: C0795688
Disease: Subarachnoid Hemorrhage, Intracranial
Subarachnoid Hemorrhage, Intracranial 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Pathologic Function 8 0.300 None 1.000 1 2018 2018
CUI: C0276655
Disease: Infection by Aspergillus fumigatus
Infection by Aspergillus fumigatus 		disease Infections Disease or Syndrome 11 0.010 None 1.000 1 2019 2019
CUI: C4476477
Disease: Human Granulocytic Anaplasmosis
Human Granulocytic Anaplasmosis 		disease Infections; Animal Diseases Disease or Syndrome 11 0.010 None 1.000 1 2004 2004
CUI: C4268744
Disease: Atypical femoral fracture
Atypical femoral fracture 		phenotype Pathologic Function 12 23 0.100 None 1.000 1 1 2019 2019
CUI: C0242287
Disease: Isaacs syndrome
Isaacs syndrome 		disease Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 13 9 0.030 None 0.667 3 2017 2019
CUI: C0266316
Disease: Congenital hydronephrosis
Congenital hydronephrosis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Congenital Abnormality 15 0.010 None 1.000 1 2018 2018
CUI: C3887527
Disease: Fused cervical vertebrae
Fused cervical vertebrae 		disease Congenital Abnormality 15 2 0.100 None 0
CUI: C0575090
Disease: Equilibration disorder
Equilibration disorder 		phenotype Nervous System Diseases Sign or Symptom 22 1 0.010 None 1.000 1 2019 2019
CUI: C3899503
Disease: Congenital hypogonadotropic hypogonadism
Congenital hypogonadotropic hypogonadism 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases Disease or Syndrome 23 10 0.010 None 1.000 1 2018 2018
CUI: C0032768
Disease: Postherpetic neuralgia
Postherpetic neuralgia 		disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 24 1 0.010 None 1.000 1 2019 2019
CUI: C1563716
Disease: Thyroid Dysgenesis
Thyroid Dysgenesis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases Congenital Abnormality 24 5 0.010 None 1.000 1 2015 2015
CUI: C0085119
Disease: Foot Ulcer
Foot Ulcer 		disease Skin and Connective Tissue Diseases Disease or Syndrome 25 3 0.010 None 1.000 1 2017 2017