NOS3, nitric oxide synthase 3, 4846

N. diseases: 706; N. variants: 39
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: C0033687
Disease: Proteinuria
Proteinuria
phenotype Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Finding 239 20 0.100 None 0
CUI: C1865903
Disease: Long-tract signs
Long-tract signs
phenotype Finding 9 0.100 None 0
Neurofibrillary degeneration (morphologic abnormality)
phenotype Cell or Molecular Dysfunction 21 0.100 None 0
Posterior Choroidal Artery Infarction
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 11 0.300 None 0
Cerebral Infarction, Right Hemisphere
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 11 0.300 None 0
Anterior Choroidal Artery Infarction
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 11 0.300 None 0
CUI: C0751014
Disease: Subcortical Infarction
Subcortical Infarction
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 13 0.300 None 0
CORONARY ARTERY SPASM 1, SUSCEPTIBILITY TO
phenotype Finding 1 1 0.100 None 0 1
CUI: C0036572
Disease: Seizures
Seizures
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 2152 553 0.100 None 0
CUI: C0242422
Disease: Parkinsonian Disorders
Parkinsonian Disorders
group Nervous System Diseases Disease or Syndrome 373 95 0.100 None 0
Cerebral Infarction, Left Hemisphere
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 11 0.300 None 0
CUI: C1840375
Disease: Elevated diastolic blood pressure
Elevated diastolic blood pressure
phenotype Cardiovascular Diseases Finding 14 1 0.100 None 0
CUI: C1848701
Disease: Elevated hepatic transaminase
Elevated hepatic transaminase
phenotype Finding 212 9 0.100 None 0
CUI: C1840374
Disease: Elevated systolic blood pressure
Elevated systolic blood pressure
phenotype Cardiovascular Diseases Finding 14 1 0.100 None 0
CUI: C0013604
Disease: Edema
Edema
phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 126 1 0.100 None 0
CUI: C4703620
Disease: Decreased level of GABA in serum
Decreased level of GABA in serum
phenotype Finding 6 0.100 None 0
CUI: C1840376
Disease: Elevated mean arterial pressure
Elevated mean arterial pressure
phenotype Cardiovascular Diseases Finding 10 1 0.100 None 0
CUI: C1273976
Disease: First myocardial infarction
First myocardial infarction
disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 17 7 0.010 None < 0.001 1 1 2009 2009
CUI: C0018681
Disease: Headache
Headache
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 338 75 0.010 None < 0.001 1 2010 2010
Secondary malignant neoplasm of bone
disease Pathological Conditions, Signs and Symptoms; Neoplasms; Musculoskeletal Diseases Neoplastic Process 647 18 0.010 None < 0.001 1 2011 2011
CUI: C0042170
Disease: Uveomeningoencephalitic Syndrome
Uveomeningoencephalitic Syndrome
disease Eye Diseases; Immune System Diseases; Nervous System Diseases Disease or Syndrome 102 27 0.010 None < 0.001 1 2 2016 2016
CUI: C0085119
Disease: Foot Ulcer
Foot Ulcer
disease Skin and Connective Tissue Diseases Disease or Syndrome 25 3 0.010 None < 0.001 1 1 2010 2010
CUI: C3149841
Disease: POLYCYSTIC KIDNEY DISEASE 1
POLYCYSTIC KIDNEY DISEASE 1
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 39 134 0.010 None < 0.001 1 1 2003 2003
CUI: C1292778
Disease: Chronic myeloproliferative disorder
Chronic myeloproliferative disorder
disease Neoplasms; Hemic and Lymphatic Diseases Neoplastic Process 366 47 0.010 None < 0.001 1 2017 2017
CUI: C0152169
Disease: Renal Colic
Renal Colic
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 5 2 0.010 None < 0.001 1 2018 2018