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.
Corticosterone Methyl Oxidase Type I Deficiency
disease Endocrine System Diseases Disease or Syndrome 4 2 0.710 limited 1.000 4 2 1997 2014
Corticosterone Methyl Oxidase Type II Deficiency
disease Disease or Syndrome 4 6 0.610 limited 1.000 7 6 1992 2014
CUI: C1384514
Disease: Conn Syndrome
Conn Syndrome
disease Endocrine System Diseases Disease or Syndrome 82 25 0.400 None 0.935 31 1 1990 2019
Glucocorticoid-remediable aldosteronism
disease Endocrine System Diseases Disease or Syndrome 30 2 0.400 None 1.000 23 1992 2019
CUI: C0020428
Disease: Hyperaldosteronism
Hyperaldosteronism
disease Endocrine System Diseases Disease or Syndrome 84 6 0.400 None 0.947 19 1996 2017
CUI: C0020595
Disease: Hypoaldosteronism
Hypoaldosteronism
disease Endocrine System Diseases Disease or Syndrome 18 0.370 None 1.000 8 1998 2013
CUI: C0033578
Disease: Prostatic Neoplasms
Prostatic Neoplasms
group Neoplasms; Male Urogenital Diseases Neoplastic Process 1722 31 0.300 None 1.000 1 2015 2015
CUI: C0376185
Disease: Hypoaldosteronism, Hyporeninemic
Hypoaldosteronism, Hyporeninemic
disease Endocrine System Diseases Disease or Syndrome 3 0.300 None 1.000 1 2001 2001
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
disease Neoplasms; Male Urogenital Diseases Neoplastic Process 4502 1082 0.300 None 1.000 1 2015 2015
CUI: C4275180
Disease: Familial hypoaldosteronism
Familial hypoaldosteronism
disease Endocrine System Diseases Disease or Syndrome 1 0.300 None 0
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
group Cardiovascular Diseases Disease or Syndrome 2322 1085 0.200 None 0.969 98 9 1992 2019
CUI: C0701163
Disease: Adrenogenital disorder
Adrenogenital disorder
disease Endocrine System Diseases Disease or Syndrome 2 0.200 None 1.000 1 2009 2009
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
group Cardiovascular Diseases Disease or Syndrome 1756 711 0.130 None 1.000 4 1 2002 2019
CUI: C0001627
Disease: Congenital adrenal hyperplasia
Congenital adrenal hyperplasia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases Disease or Syndrome 87 36 0.130 None 1.000 3 1 2001 2004
CUI: C0015544
Disease: Failure to Thrive
Failure to Thrive
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 842 10 0.120 None 1.000 2 1994 1999
CUI: C0032914
Disease: Pre-Eclampsia
Pre-Eclampsia
phenotype Female Urogenital Diseases and Pregnancy Complications Pathologic Function 166 14 0.110 None 1.000 1 2004 2004
CUI: C0020625
Disease: Hyponatremia
Hyponatremia
phenotype Nutritional and Metabolic Diseases Disease or Syndrome 109 11 0.110 None 1.000 1 1994 1994
CUI: C1621895
Disease: Adrenal hyperplasia
Adrenal hyperplasia
disease Pathological Conditions, Signs and Symptoms; Neoplasms; Endocrine System Diseases Disease or Syndrome 33 0.110 None 1.000 1 2001 2001
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
disease Cardiovascular Diseases Disease or Syndrome 445 293 0.100 None 0.949 39 4 1995 2018
CUI: C0009777
Disease: Conn Adenoma
Conn Adenoma
disease Neoplasms; Endocrine System Diseases Neoplastic Process 107 5 0.100 None 1.000 29 1995 2019
CUI: C0001430
Disease: Adenoma
Adenoma
group Neoplasms Neoplastic Process 1183 103 0.100 None 0.944 18 1 2000 2019
CUI: C0027651
Disease: Neoplasms
Neoplasms
group Neoplasms Neoplastic Process 10161 1644 0.100 None 1.000 15 1991 2019
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure
disease Cardiovascular Diseases Disease or Syndrome 1760 165 0.100 None 1.000 14 1 2002 2017
CUI: C4289986
Disease: Aldosterone Synthase Deficiency
Aldosterone Synthase Deficiency
disease Endocrine System Diseases Disease or Syndrome 1 3 0.100 None 1.000 10 3 1999 2019
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
phenotype Clinical Attribute 843 1931 0.100 None 1.000 3 3 2018 2019