GH1, growth hormone 1, 2688

N. diseases: 686; N. variants: 27
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: C0342257
Disease: Complications of Diabetes Mellitus
Complications of Diabetes Mellitus
group Endocrine System Diseases Disease or Syndrome 240 35 0.010 None 1.000 1 2003 2003
CUI: C0342326
Disease: Tumor-induced hypoglycemia
Tumor-induced hypoglycemia
disease Disease or Syndrome 4 0.010 None 1.000 1 1989 1989
CUI: C0342409
Disease: Hypophysitis
Hypophysitis
disease Nervous System Diseases; Endocrine System Diseases Disease or Syndrome 19 0.010 None 1.000 1 2020 2020
CUI: C0333519
Disease: Caries (morphologic abnormality)
Caries (morphologic abnormality)
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 106 33 0.010 None < 0.001 1 2018 2018
CUI: C0278879
Disease: Childhood Burkitt Lymphoma
Childhood Burkitt Lymphoma
disease Neoplasms; Infections; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 477 7 0.010 None 1.000 1 1993 1993
Constitutional delay of growth and puberty
disease Disease or Syndrome 16 7 0.010 None 1.000 1 2019 2019
CUI: C0342543
Disease: Central Precocious Puberty
Central Precocious Puberty
disease Endocrine System Diseases Disease or Syndrome 32 2 0.010 None 1.000 1 2017 2017
CUI: C0278877
Disease: Adult Meningioma
Adult Meningioma
disease Neoplasms; Nervous System Diseases Neoplastic Process 405 30 0.010 None 1.000 1 2019 2019
CUI: C0342162
Disease: Compensated hypothyroidism
Compensated hypothyroidism
disease Endocrine System Diseases Disease or Syndrome 7 1 0.010 None 1.000 1 2001 2001
CUI: C0342134
Disease: T>3< thyrotoxicosis
T>3< thyrotoxicosis
disease Endocrine System Diseases Disease or Syndrome 1 0.010 None 1.000 1 2017 2017
CUI: C0333317
Disease: Fibrous body
Fibrous body
disease Acquired Abnormality 3 0.010 None 1.000 1 2010 2010
CUI: C0312414
Disease: Menstrual spotting
Menstrual spotting
phenotype Sign or Symptom 27 2 0.010 None 1.000 1 2008 2008
CUI: C0333983
Disease: Hyperplastic Polyp
Hyperplastic Polyp
disease Pathological Conditions, Signs and Symptoms Neoplastic Process 204 22 0.010 None 1.000 1 2010 2010
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications Neoplastic Process 1881 283 0.010 None 1.000 1 2008 2008
CUI: C0338106
Disease: Adenocarcinoma of colon
Adenocarcinoma of colon
disease Digestive System Diseases; Neoplasms Neoplastic Process 406 10 0.010 None 1.000 1 2016 2016
CUI: C0338503
Disease: Septo-Optic Dysplasia
Septo-Optic Dysplasia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 35 19 0.010 None 1.000 1 2002 2002
CUI: C0339543
Disease: Epiretinal Membrane
Epiretinal Membrane
disease Eye Diseases Acquired Abnormality 102 0.010 None 1.000 1 2009 2009
CUI: C0340987
Disease: Splenic atrophy
Splenic atrophy
disease Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases Disease or Syndrome 4 0.010 None 1.000 1 2018 2018
CUI: C0300948
Disease: Caudal Regression Syndrome
Caudal Regression Syndrome
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases Congenital Abnormality 12 1 0.010 None 1.000 1 2017 2017
CUI: C0341318
Disease: Enterocutaneous Fistula
Enterocutaneous Fistula
disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Anatomical Abnormality 8 1 0.010 None 1.000 1 2019 2019
CUI: C0282201
Disease: Phosphate Diabetes
Phosphate Diabetes
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 51 0.010 None 1.000 1 2008 2008
CUI: C0342410
Disease: Autoimmune Hypophysitis
Autoimmune Hypophysitis
disease Immune System Diseases; Nervous System Diseases; Endocrine System Diseases Disease or Syndrome 5 0.010 None 1.000 1 1999 1999
CUI: C0342853
Disease: Sialuria
Sialuria
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 11 17 0.010 None 1.000 1 2001 2001
CUI: C0432230
Disease: Langer Mesomelic Dysplasia Syndrome
Langer Mesomelic Dysplasia Syndrome
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 12 4 0.010 None 1.000 1 2009 2009
CUI: C0432411
Disease: Chromosome 9, trisomy
Chromosome 9, trisomy
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 12 0.010 None 1.000 1 2010 2010