NBEAL1, neurobeachin like 1, 65065

N. diseases: 60; N. variants: 24
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: C0546999
Disease: Larva Migrans, Cutaneous
Larva Migrans, Cutaneous
disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 1 0.010 None 1.000 1 2018 2018
CUI: C0272339
Disease: Prekallikrein deficiency
Prekallikrein deficiency
disease Hemic and Lymphatic Diseases Disease or Syndrome 5 6 0.010 None 1.000 1 1986 1986
CUI: C0233407
Disease: Disorientation
Disorientation
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms Sign or Symptom 12 0.010 None 1.000 1 2018 2018
CUI: C0948268
Disease: Hemodynamic instability
Hemodynamic instability
disease Disease or Syndrome 15 0.010 None 1.000 1 2018 2018
CUI: C2712971
Disease: Enteritis due to Norovirus
Enteritis due to Norovirus
disease Infections Disease or Syndrome 16 0.010 None 1.000 1 2018 2018
Bacteremia due to Staphylococcus aureus
disease Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 17 1 0.010 None 1.000 1 2017 2017
CUI: C3534585
Disease: Infection caused by Norovirus
Infection caused by Norovirus
group Infections Disease or Syndrome 18 0.010 None 1.000 1 2018 2018
CUI: C0021832
Disease: Intestinal Diseases, Parasitic
Intestinal Diseases, Parasitic
group Digestive System Diseases; Infections Disease or Syndrome 19 0.010 None 1.000 1 2018 2018
CUI: C0205204
Disease: Scab
Scab
disease Acquired Abnormality 24 0.010 None 1.000 1 2017 2017
CUI: C4316909
Disease: Marijuana Use
Marijuana Use
disease Mental Disorders; Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 33 0.010 None 1.000 1 2018 2018
CUI: C0019269
Disease: Hermaphroditism
Hermaphroditism
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases Disease or Syndrome 34 0.010 None 1.000 1 2018 2018
CUI: C0272302
Disease: Gray Platelet Syndrome
Gray Platelet Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 38 14 0.010 None 1.000 1 2018 2018
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement
phenotype Laboratory Procedure 39 568 0.100 None 1.000 1 20 2011 2011
CUI: C1695782
Disease: Cerebral hypoperfusion
Cerebral hypoperfusion
disease Disease or Syndrome 40 1 0.010 None 1.000 1 2020 2020
CUI: C0007965
Disease: Chediak-Higashi Syndrome
Chediak-Higashi Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 41 14 0.010 None 1.000 1 2014 2014
CUI: C1443924
Disease: Severe diarrhea
Severe diarrhea
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 47 6 0.010 None 1.000 1 2011 2011
CUI: C0011127
Disease: Pressure Ulcer
Pressure Ulcer
disease Skin and Connective Tissue Diseases Disease or Syndrome 49 1 0.010 None 1.000 1 2017 2017
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 59 125 0.010 None 1.000 1 1985 1985
CUI: C0018889
Disease: Helminthiasis
Helminthiasis
disease Infections Disease or Syndrome 59 1 0.010 None 1.000 1 2018 2018
CUI: C0025229
Disease: Melioidosis
Melioidosis
disease Infections Disease or Syndrome 65 9 0.010 None 1.000 1 2018 2018
CUI: C1285498
Disease: Vegetation
Vegetation
disease Anatomical Abnormality 67 0.020 None 1.000 2 2017 2019
CUI: C0153252
Disease: Systemic candidiasis
Systemic candidiasis
disease Infections Disease or Syndrome 73 0.010 None 1.000 1 2001 2001
CUI: C0037278
Disease: Skin Diseases, Infectious
Skin Diseases, Infectious
group Infections; Skin and Connective Tissue Diseases Disease or Syndrome 74 0.010 None 1.000 1 2018 2018
CUI: C0009676
Disease: Confusion
Confusion
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 75 5 0.010 None 1.000 1 2018 2018
CUI: C0815107
Disease: psychological distress
psychological distress
disease Mental or Behavioral Dysfunction 87 10 0.010 None 1.000 1 2017 2017