GYPA, glycophorin A (MNS blood group), 2993

N. diseases: 136; N. variants: 5
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: C3900051
Disease: Amotivation
Amotivation 		phenotype Sign or Symptom 2 0.010 None 1.000 1 2020 2020
CUI: C1971635
Disease: Scleritis and episcleritis (disorder)
Scleritis and episcleritis (disorder) 		phenotype Pathological Conditions, Signs and Symptoms; Eye Diseases Disease or Syndrome 3 0.010 None 1.000 1 2019 2019
CUI: C4733575
Disease: newly diagnosed non-small cell lung cancer
newly diagnosed non-small cell lung cancer 		disease Neoplastic Process 4 3 0.010 None 1.000 1 2018 2018
CUI: C0750992
Disease: Catatonia, Malignant
Catatonia, Malignant 		disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms Disease or Syndrome 5 0.010 None 1.000 1 2017 2017
CUI: C0268225
Disease: Aspartylglucosaminuria
Aspartylglucosaminuria 		phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 9 53 0.010 None 1.000 1 1990 1990
CUI: C0349653
Disease: Congenital disorder of glycosylation type 1A
Congenital disorder of glycosylation type 1A 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 10 80 0.010 None 1.000 1 2001 2001
CUI: C0920372
Disease: Carcinogenesis, Radiation
Carcinogenesis, Radiation 		phenotype Pathological Conditions, Signs and Symptoms; Neoplasms Neoplastic Process 13 0.010 None 1.000 1 1996 1996
CUI: C1862839
Disease: Anterior segment mesenchymal dysgenesis
Anterior segment mesenchymal dysgenesis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 13 2 0.010 None 1.000 1 1982 1982
CUI: C1263988
Disease: Hemolytic disorder
Hemolytic disorder 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 15 0.010 None 1.000 1 2018 2018
CUI: C0014761
Disease: Erythroblastosis, Fetal
Erythroblastosis, Fetal 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 16 1 0.010 None 1.000 1 1987 1987
CUI: C4551511
Disease: X-linked sideroblastic anemia
X-linked sideroblastic anemia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 16 23 0.010 None 1.000 1 1992 1992
CUI: C0234935
Disease: Acute urticaria
Acute urticaria 		disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 17 0.010 None < 0.001 1 1979 1979
CUI: C4317295
Disease: Congenital disorder of glycosylation type 1s
Congenital disorder of glycosylation type 1s 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 19 0.010 None 1.000 1 2001 2001
CUI: C0022716
Disease: Menkes Kinky Hair Syndrome
Menkes Kinky Hair Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Nervous System Diseases Disease or Syndrome 20 99 0.010 None 1.000 1 1989 1989
CUI: C0025237
Disease: Melnick-Needles Syndrome
Melnick-Needles Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 23 19 0.020 None 1.000 2 2010 2018
CUI: C1704380
Disease: Distal Renal Tubular Acidosis
Distal Renal Tubular Acidosis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 23 18 0.010 None 1.000 1 1998 1998
CUI: C0302314
Disease: Xanthoma
Xanthoma 		disease Nutritional and Metabolic Diseases Disease or Syndrome 29 4 0.010 None 1.000 1 2017 2017
CUI: C0041466
Disease: Typhoid Fever
Typhoid Fever 		disease Infections Disease or Syndrome 31 5 0.010 None 1.000 1 1993 1993
CUI: C0085635
Disease: Photopsia
Photopsia 		phenotype Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Disease or Syndrome 35 0.010 None 1.000 1 2017 2017
CUI: C0008728
Disease: Eosinophilic granulomatosis with polyangiitis
Eosinophilic granulomatosis with polyangiitis 		disease Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases Disease or Syndrome 38 3 0.010 None 1.000 1 2015 2015
CUI: C0008060
Disease: child abuse behavior
child abuse behavior 		phenotype Mental or Behavioral Dysfunction 40 11 0.010 None 1.000 1 2017 2017
CUI: C0085652
Disease: Pyoderma Gangrenosum
Pyoderma Gangrenosum 		disease Skin and Connective Tissue Diseases Disease or Syndrome 47 2 0.010 None 1.000 1 2017 2017
CUI: C0233523
Disease: Antisocial behavior
Antisocial behavior 		phenotype Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 51 17 0.010 None 1.000 1 2009 2009
CUI: C0037889
Disease: Hereditary spherocytosis
Hereditary spherocytosis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 53 13 0.020 None 1.000 2 2008 2009
CUI: C1258104
Disease: Diffuse Scleroderma
Diffuse Scleroderma 		disease Skin and Connective Tissue Diseases Disease or Syndrome 56 5 0.010 None 1.000 1 2005 2005