GYPC, glycophorin C (Gerbich blood group), 2995

N. diseases: 55; N. variants: 2
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: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
phenotype Neoplastic Process 6626 169 0.030 None 1.000 3 1996 2008
CUI: C0871189
Disease: Psychotic symptom
Psychotic symptom
phenotype Sign or Symptom 86 21 0.010 None 1.000 1 2013 2013
CUI: C0427480
Disease: Elliptocytosis found
Elliptocytosis found
phenotype Finding 12 0.100 None 0
CUI: C0677598
Disease: Stomatocytosis Result
Stomatocytosis Result
phenotype Laboratory or Test Result 13 0.100 None 0
Increased red cell osmotic fragility
phenotype Finding 9 0.100 None 0
CUI: C1859778
Disease: Postnatal growth retardation
Postnatal growth retardation
phenotype Finding 121 11 0.100 None 0
GERBICH BLOOD GROUP SYSTEM, GERBICH PHENOTYPE
phenotype Finding 1 1 0.100 None 0 1
CUI: C0011570
Disease: Mental Depression
Mental Depression
disease Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 1478 271 0.010 None 1.000 1 2017 2017
CUI: C0344315
Disease: Depressed mood
Depressed mood
phenotype Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 1461 269 0.010 None 1.000 1 2017 2017
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
disease Cardiovascular Diseases Disease or Syndrome 2006 267 0.010 None 1.000 1 2018 2018
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
disease Cardiovascular Diseases Disease or Syndrome 2044 281 0.010 None 1.000 1 2018 2018
CUI: C0013902
Disease: Elliptocytosis, Hereditary
Elliptocytosis, Hereditary
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 23 1 0.420 None 1.000 3 1991 2001
Ovalocytosis, Malaysian-Melanesian-Filipino Type
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 9 5 0.020 None 1.000 2 2004 2011
CUI: C0002881
Disease: Anemia, Hemolytic, Congenital
Anemia, Hemolytic, Congenital
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 27 8 0.100 None 0
CUI: C0221354
Disease: Frontal bossing
Frontal bossing
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Congenital Abnormality 321 22 0.100 None 0
CUI: C0008350
Disease: Cholelithiasis
Cholelithiasis
disease Digestive System Diseases Disease or Syndrome 252 90 0.100 None 0
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
disease Digestive System Diseases; Neoplasms Neoplastic Process 5725 942 0.010 None 1.000 1 2013 2013
CUI: C0009769
Disease: Conjunctivitis, Giant Papillary
Conjunctivitis, Giant Papillary
disease Eye Diseases; Immune System Diseases Disease or Syndrome 1 0.010 None 1.000 1 2007 2007
CUI: C0022577
Disease: Keratoconjunctivitis, Vernal
Keratoconjunctivitis, Vernal
disease Eye Diseases; Immune System Diseases Disease or Syndrome 40 0.010 None 1.000 1 2007 2007
CUI: C1274788
Disease: Atopic keratoconjunctivitis
Atopic keratoconjunctivitis
disease Eye Diseases; Immune System Diseases Disease or Syndrome 9 0.010 None 1.000 1 2007 2007
CUI: C0039128
Disease: Syphilis
Syphilis
disease Female Urogenital Diseases and Pregnancy Complications; Infections; Male Urogenital Diseases Disease or Syndrome 80 3 0.010 None 1.000 1 2003 2003
CUI: C0272048
Disease: stomatocytic anemia
stomatocytic anemia
disease Hemic and Lymphatic Diseases Disease or Syndrome 15 1 0.100 None 0
CUI: C0024530
Disease: Malaria
Malaria
disease Infections Disease or Syndrome 685 148 0.320 None 1.000 2 2001 2004
CUI: C0019097
Disease: Hemorrhagic Fever, Argentinian
Hemorrhagic Fever, Argentinian
disease Infections Disease or Syndrome 9 0.010 None 1.000 1 2017 2017
CUI: C0024537
Disease: Malaria, Vivax
Malaria, Vivax
disease Infections Disease or Syndrome 60 2 0.010 None 1.000 1 2014 2014