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: 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: C4015913
Disease: GERBICH BLOOD GROUP SYSTEM, GERBICH PHENOTYPE
GERBICH BLOOD GROUP SYSTEM, GERBICH PHENOTYPE 		phenotype Finding 1 1 0.100 None 0 1
CUI: C1862322
Disease: Ovalocytosis, Malaysian-Melanesian-Filipino Type
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: C0019097
Disease: Hemorrhagic Fever, Argentinian
Hemorrhagic Fever, Argentinian 		disease Infections Disease or Syndrome 9 0.010 None 1.000 1 2017 2017
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: C1849478
Disease: Increased red cell osmotic fragility
Increased red cell osmotic fragility 		phenotype Finding 9 0.100 None 0
CUI: C0241982
Disease: Bulla of lung
Bulla of lung 		disease Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Disease or Syndrome 11 2 0.010 None 1.000 1 1998 1998
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
CUI: C0272048
Disease: stomatocytic anemia
stomatocytic anemia 		disease Hemic and Lymphatic Diseases Disease or Syndrome 15 1 0.100 None 0
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
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: C0043395
Disease: Yellow Fever
Yellow Fever 		disease Infections Disease or Syndrome 28 0.010 None 1.000 1 2006 2006
CUI: C0857007
Disease: Hyperbilirubinemia, Neonatal
Hyperbilirubinemia, Neonatal 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 33 15 0.100 None 0
CUI: C0085593
Disease: Chills
Chills 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 34 0.100 None 0
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: C0206160
Disease: Reticulocytosis
Reticulocytosis 		phenotype Pathological Conditions, Signs and Symptoms Finding 40 1 0.100 None 0
CUI: C1859236
Disease: Prolonged neonatal jaundice
Prolonged neonatal jaundice 		phenotype Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities Finding 59 14 0.100 None 0
CUI: C0024537
Disease: Malaria, Vivax
Malaria, Vivax 		disease Infections Disease or Syndrome 60 2 0.010 None 1.000 1 2014 2014
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: C0871189
Disease: Psychotic symptom
Psychotic symptom 		phenotype Sign or Symptom 86 21 0.010 None 1.000 1 2013 2013
CUI: C0020305
Disease: Hydrops Fetalis
Hydrops Fetalis 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 92 14 0.100 None 0
CUI: C1859778
Disease: Postnatal growth retardation
Postnatal growth retardation 		phenotype Finding 121 11 0.100 None 0
CUI: C0153014
Disease: Non-arthropod borne lymphocytic choriomeningitis
Non-arthropod borne lymphocytic choriomeningitis 		disease Infections; Nervous System Diseases Disease or Syndrome 133 0.010 None 1.000 1 2014 2014
CUI: C0024266
Disease: Lymphocytic Choriomeningitis
Lymphocytic Choriomeningitis 		disease Infections; Nervous System Diseases Disease or Syndrome 147 0.010 None 1.000 1 2014 2014