SERPINA6, serpin family A member 6, 866

N. diseases: 68; N. variants: 4
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.
Other specified disorders of adrenal gland
disease Endocrine System Diseases Disease or Syndrome 1 0.200 None 1.000 2 2006 2010
Abnormality of cortisol-binding globulin
disease Endocrine System Diseases Disease or Syndrome 1 0.200 None 1.000 2 2006 2010
Corticosteroid-Binding Globulin, Elevated
disease Hemic and Lymphatic Diseases Disease or Syndrome 1 0.200 None 1.000 2 2006 2010
Corticosteroid-Binding Globulin Deficiency
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 3 2 0.950 None 1.000 10 2 1992 2019
CUI: C4727182
Disease: Recurrent Cushing Disease
Recurrent Cushing Disease
disease Nervous System Diseases; Endocrine System Diseases Disease or Syndrome 6 0.010 None 1.000 1 2017 2017
CUI: C4025573
Disease: Increased muscle fatiguability
Increased muscle fatiguability
phenotype Finding 9 3 0.100 None 0
CUI: C0271583
Disease: ACTH Deficiency, Isolated
ACTH Deficiency, Isolated
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Endocrine System Diseases Disease or Syndrome 11 11 0.010 None 1.000 1 2001 2001
Hypocortisolism secondary to another disorder
disease Endocrine System Diseases Disease or Syndrome 13 0.010 None 1.000 1 2012 2012
CUI: C3178789
Disease: Widespread Chronic Pain
Widespread Chronic Pain
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 19 12 0.010 None 1.000 1 2010 2010
CUI: C0685787
Disease: Cleft face
Cleft face
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 23 0.010 None 1.000 1 2011 2011
CUI: C0405580
Disease: Adrenal cortical hypofunction
Adrenal cortical hypofunction
disease Endocrine System Diseases Disease or Syndrome 52 5 0.010 None 1.000 1 2018 2018
CUI: C3714534
Disease: dowling-degos disease
dowling-degos disease
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 53 7 0.010 None 1.000 1 2006 2006
CUI: C0221074
Disease: Depression, Postpartum
Depression, Postpartum
disease Female Urogenital Diseases and Pregnancy Complications; Mental Disorders Mental or Behavioral Dysfunction 54 6 0.010 None 1.000 1 2019 2019
Pauci-immune Glomerulonephritis associated with Granulomatosis with Polyangiitis
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 71 15 0.010 None 1.000 1 2001 2001
CUI: C0001623
Disease: Adrenal gland hypofunction
Adrenal gland hypofunction
phenotype Endocrine System Diseases Disease or Syndrome 90 10 0.010 None 1.000 1 2018 2018
Congenital Disorders of Glycosylation
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 102 38 0.010 None 1.000 1 2019 2019
Pituitary-dependent Cushing's disease
disease Nervous System Diseases; Endocrine System Diseases Disease or Syndrome 115 8 0.020 None 1.000 2 2017 2017
CUI: C0015674
Disease: Chronic Fatigue Syndrome
Chronic Fatigue Syndrome
disease Infections; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 118 14 0.020 None 1.000 2 2004 2007
CUI: C0342443
Disease: Adrenal Cushing's syndrome
Adrenal Cushing's syndrome
disease Endocrine System Diseases Disease or Syndrome 120 9 0.010 None 1.000 1 2017 2017
CUI: C0020649
Disease: Hypotension
Hypotension
phenotype Cardiovascular Diseases Finding 125 2 0.100 None 0
CUI: C0010481
Disease: Cushing Syndrome
Cushing Syndrome
disease Endocrine System Diseases Disease or Syndrome 126 9 0.010 None 1.000 1 2017 2017
CUI: C3495801
Disease: Granulomatosis with polyangiitis
Granulomatosis with polyangiitis
disease Respiratory Tract Diseases; Immune System Diseases; Cardiovascular Diseases Disease or Syndrome 126 18 0.010 None 1.000 1 2001 2001
Abnormality of metabolism/homeostasis
phenotype Finding 171 5 0.100 None 0
CUI: C0150055
Disease: Chronic pain
Chronic pain
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 207 19 0.010 None 1.000 1 2012 2012
CUI: C0018939
Disease: Hematological Disease
Hematological Disease
group Hemic and Lymphatic Diseases Disease or Syndrome 255 16 0.010 None 1.000 1 1980 1980