ADRA2B, adrenoceptor alpha 2B, 151

N. diseases: 296; N. variants: 9
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: C3552824
Disease: Enhancement of the C-reflex
Enhancement of the C-reflex 		phenotype Finding 2 0.100 None 0
CUI: C3552825
Disease: Jerk-locked premyoclonus spikes
Jerk-locked premyoclonus spikes 		phenotype Finding 2 0.100 None 0
CUI: C1842852
Disease: EPILEPSY, MYOCLONIC, BENIGN ADULT FAMILIAL, TYPE 2
EPILEPSY, MYOCLONIC, BENIGN ADULT FAMILIAL, TYPE 2 		disease Nervous System Diseases Disease or Syndrome 3 0.310 moderate 1.000 2 2001 2019
CUI: C3552821
Disease: EEG with photoparoxysmal response
EEG with photoparoxysmal response 		phenotype Finding 3 1 0.100 None 0
CUI: C1832841
Disease: EPILEPSY, FAMILIAL ADULT MYOCLONIC, 1
EPILEPSY, FAMILIAL ADULT MYOCLONIC, 1 		disease Nervous System Diseases Disease or Syndrome 4 0.300 None 1.000 1 2014 2014
CUI: C3806961
Disease: Giant somatosensory evoked potentials
Giant somatosensory evoked potentials 		phenotype Finding 4 0.100 None 0
CUI: C4025792
Disease: EEG with irregular generalized spike and wave complexes
EEG with irregular generalized spike and wave complexes 		phenotype Finding 7 1 0.100 None 0
CUI: C0241893
Disease: Tick fever
Tick fever 		disease Infections; Animal Diseases Disease or Syndrome 9 0.010 None 1.000 1 2019 2019
CUI: C0276849
Disease: Infection by Babesia bovis
Infection by Babesia bovis 		disease Infections; Animal Diseases Disease or Syndrome 9 0.010 None 1.000 1 2019 2019
CUI: C0340291
Disease: Silent myocardial ischemia
Silent myocardial ischemia 		disease Cardiovascular Diseases Disease or Syndrome 9 4 0.010 None 1.000 1 2010 2010
CUI: C1274989
Disease: Retinoid dermatitis
Retinoid dermatitis 		disease Skin and Connective Tissue Diseases; Immune System Diseases; Chemically-Induced Disorders Disease or Syndrome 9 0.010 None 1.000 1 2019 2019
CUI: C0157743
Disease: Vibratory urticaria
Vibratory urticaria 		disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 10 1 0.010 None 1.000 1 2018 2018
CUI: C0597854
Disease: renin induced hypertension
renin induced hypertension 		disease Disease or Syndrome 11 0.010 None 1.000 1 2019 2019
CUI: C3279470
Disease: HYPOTRICHOSIS 8
HYPOTRICHOSIS 8 		disease Skin and Connective Tissue Diseases Disease or Syndrome 13 8 0.010 None 1.000 1 2008 2008
CUI: C1845202
Disease: Nephrogenic Syndrome of Inappropriate Antidiuresis
Nephrogenic Syndrome of Inappropriate Antidiuresis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Endocrine System Diseases Disease or Syndrome 14 4 0.010 None 1.000 1 2019 2019
CUI: C1535964
Disease: Cholestatic pruritus
Cholestatic pruritus 		phenotype Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Sign or Symptom 15 0.010 None 1.000 1 2019 2019
CUI: C0936282
Disease: Blastoma
Blastoma 		disease Neoplasms Neoplastic Process 20 0.010 None 1.000 1 1996 1996
CUI: C0033117
Disease: Priapism
Priapism 		disease Male Urogenital Diseases Disease or Syndrome 22 2 0.010 None 1.000 1 2018 2018
CUI: C4304832
Disease: Primary pigmented nodular adrenocortical disease
Primary pigmented nodular adrenocortical disease 		disease Disease or Syndrome 22 1 0.010 None 1.000 1 2012 2012
CUI: C1334386
Disease: Meningeal melanoma
Meningeal melanoma 		disease Neoplastic Process 23 1 0.010 None 1.000 1 2019 2019
CUI: C1809471
Disease: Familial benign hypercalcemia
Familial benign hypercalcemia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Endocrine System Diseases Disease or Syndrome 24 35 0.010 None 1.000 1 2010 2010
CUI: C3839460
Disease: Nonprogressive
Nonprogressive 		phenotype Finding 24 0.100 None 0
CUI: C0342494
Disease: Adrenocortical hyperplasia
Adrenocortical hyperplasia 		disease Endocrine System Diseases Disease or Syndrome 25 0.010 None 1.000 1 2010 2010
CUI: C1299624
Disease: Postural Orthostatic Tachycardia Syndrome
Postural Orthostatic Tachycardia Syndrome 		disease Nervous System Diseases Disease or Syndrome 25 1 0.010 None 1.000 1 2019 2019
CUI: C3178766
Disease: Nociceptive Pain
Nociceptive Pain 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 25 0.010 None 1.000 1 2017 2017