ADRA1A, adrenoceptor alpha 1A, 148

N. diseases: 294; N. variants: 30
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: 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: 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: C3150943
Disease: Long Qt Syndrome 2
Long Qt Syndrome 2
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Disease or Syndrome 13 267 0.010 None 1.000 1 2009 2009
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
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 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: C0042420
Disease: Vasovagal syncope
Vasovagal syncope
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 16 1 0.010 None 1.000 1 1 2014 2014
CUI: C0936282
Disease: Blastoma
Blastoma
disease Neoplasms Neoplastic Process 20 0.010 None 1.000 1 1996 1996
CUI: C0600520
Disease: Left Ventricle Remodeling
Left Ventricle Remodeling
phenotype Pathological Conditions, Signs and Symptoms Organ or Tissue Function 21 0.300 None 1.000 1 2010 2010
CUI: C0033117
Disease: Priapism
Priapism
disease Male Urogenital Diseases Disease or Syndrome 22 2 0.010 None 1.000 1 2018 2018
Primary pigmented nodular adrenocortical disease
disease Disease or Syndrome 22 1 0.010 None 1.000 1 2012 2012
CUI: C0232849
Disease: Bladder pain
Bladder pain
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 23 0.010 None 1.000 1 2017 2017
CUI: C1334386
Disease: Meningeal melanoma
Meningeal melanoma
disease Neoplastic Process 23 1 0.010 None 1.000 1 2019 2019
CUI: C0600519
Disease: Ventricular Remodeling
Ventricular Remodeling
phenotype Pathological Conditions, Signs and Symptoms Organ or Tissue Function 24 0.300 None 1.000 1 2010 2010
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: C0342494
Disease: Adrenocortical hyperplasia
Adrenocortical hyperplasia
disease Endocrine System Diseases Disease or Syndrome 25 0.010 None 1.000 1 2010 2010
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
CUI: C0030517
Disease: Parathyroid Diseases
Parathyroid Diseases
group Endocrine System Diseases Disease or Syndrome 26 4 0.010 None 1.000 1 2011 2011
Humoral hypercalcemia of malignancy (disorder)
disease Neoplasms; Nutritional and Metabolic Diseases Disease or Syndrome 26 0.010 None 1.000 1 2018 2018
CUI: C1836672
Disease: Total Hypotrichosis, Mari type
Total Hypotrichosis, Mari type
disease Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Disease or Syndrome 27 4 0.010 None 1.000 1 2008 2008
CUI: C0264657
Disease: Renal sclerosis with hypertension
Renal sclerosis with hypertension
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Cardiovascular Diseases Disease or Syndrome 29 9 0.010 None 1.000 1 1 2009 2009