SSTR4, somatostatin receptor 4, 6754

N. diseases: 266; N. variants: 9
Source: BEFREE ×
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: C3279470
Disease: HYPOTRICHOSIS 8
HYPOTRICHOSIS 8 		disease Skin and Connective Tissue Diseases Disease or Syndrome 11 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 3 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: C0033117
Disease: Priapism
Priapism 		disease Male Urogenital Diseases Disease or Syndrome 19 2 0.010 None 1.000 1 2018 2018
CUI: C0936282
Disease: Blastoma
Blastoma 		disease Neoplasms Neoplastic Process 20 0.010 None 1.000 1 1996 1996
CUI: C4304832
Disease: Primary pigmented nodular adrenocortical disease
Primary pigmented nodular adrenocortical disease 		disease Disease or Syndrome 20 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: C3178766
Disease: Nociceptive Pain
Nociceptive Pain 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 23 0.010 None 1.000 1 2017 2017
CUI: C1299624
Disease: Postural Orthostatic Tachycardia Syndrome
Postural Orthostatic Tachycardia Syndrome 		disease Nervous System Diseases Disease or Syndrome 24 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 3 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
CUI: C0030517
Disease: Parathyroid Diseases
Parathyroid Diseases 		group Endocrine System Diseases Disease or Syndrome 26 4 0.010 None 1.000 1 2011 2011
CUI: C0149911
Disease: Humoral hypercalcemia of malignancy (disorder)
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 1 0.010 None 1.000 1 2008 2008
CUI: C4048195
Disease: Autosomal dominant hypocalcemia
Autosomal dominant hypocalcemia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 27 8 0.010 None 1.000 1 2000 2000
CUI: C0455988
Disease: Hydrops Fetalis, Non-Immune
Hydrops Fetalis, Non-Immune 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 28 1 0.010 None 1.000 1 2018 2018
CUI: C0020071
Disease: Hereditary Sensory Autonomic Neuropathy, Type 1
Hereditary Sensory Autonomic Neuropathy, Type 1 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 29 10 0.010 None 1.000 1 1999 1999
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
CUI: C0220659
Disease: Acrodysostosis
Acrodysostosis 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms Disease or Syndrome 31 6 0.020 None 1.000 2 2012 2012
CUI: C3489396
Disease: Hypogonadism, Isolated Hypogonadotropic
Hypogonadism, Isolated Hypogonadotropic 		disease Endocrine System Diseases Disease or Syndrome 31 7 0.020 None 1.000 2 2005 2007