RHAG, Rh associated glycoprotein, 6005

N. diseases: 41; N. variants: 13
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: C1861455
Disease: STOMATOCYTOSIS I
STOMATOCYTOSIS I
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 20 3 0.710 strong 1.000 5 3 1998 2013
CUI: C1849387
Disease: Rh-Null, Regulator Type
Rh-Null, Regulator Type
disease Hemic and Lymphatic Diseases Disease or Syndrome 3 9 0.700 strong 1.000 5 9 1996 2009
CUI: C0677598
Disease: Stomatocytosis Result
Stomatocytosis Result
phenotype Laboratory or Test Result 13 0.400 strong 1.000 2 1998 2009
CUI: C0272048
Disease: stomatocytic anemia
stomatocytic anemia
disease Hemic and Lymphatic Diseases Disease or Syndrome 15 1 0.400 strong 1.000 2 1998 2009
CUI: C0272052
Disease: Rh Deficiency Syndrome
Rh Deficiency Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 3 0.300 None 1.000 2 1996 1998
CUI: C0002878
Disease: Anemia, Hemolytic
Anemia, Hemolytic
disease Hemic and Lymphatic Diseases Disease or Syndrome 154 31 0.110 None 1.000 1 1 2012 2012
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
phenotype Laboratory Procedure 1156 2575 0.100 None 1.000 1 1 2018 2018
CUI: C0022346
Disease: Icterus
Icterus
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 241 17 0.100 None 0 1
CUI: C0853655
Disease: Abnormal mean corpuscular volume
Abnormal mean corpuscular volume
phenotype Finding 2 0.100 None 0
CUI: C0427437
Disease: MCH - low
MCH - low
phenotype Finding 5 0.100 None 0
CUI: C0268306
Disease: Unconjugated hyperbilirubinemia
Unconjugated hyperbilirubinemia
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 23 4 0.100 None 0 1
CUI: C0241231
Disease: splenomegaly massive
splenomegaly massive
phenotype Finding 1 1 0.100 None 0 1
CUI: C0221278
Disease: Anisocytosis
Anisocytosis
phenotype Finding 16 1 0.100 None 0
CUI: C0206160
Disease: Reticulocytosis
Reticulocytosis
phenotype Pathological Conditions, Signs and Symptoms Finding 40 1 0.100 None 0 1
CUI: C0019209
Disease: Hepatomegaly
Hepatomegaly
phenotype Pathological Conditions, Signs and Symptoms; Digestive System Diseases Finding 523 30 0.100 None 0 1
CUI: C0038002
Disease: Splenomegaly
Splenomegaly
phenotype Pathological Conditions, Signs and Symptoms Finding 345 19 0.100 None 0
CUI: C4025805
Disease: Intermittent jaundice
Intermittent jaundice
phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 3 0.100 None 0
CUI: C4025731
Disease: Abnormal thrombosis
Abnormal thrombosis
disease Anatomical Abnormality 13 1 0.100 None 0
CUI: C4025593
Disease: Increased intracellular sodium
Increased intracellular sodium
phenotype Finding 2 0.100 None 0
Increased red cell osmotic fragility
phenotype Finding 9 0.100 None 0
CUI: C2698117
Disease: Anisocyte Measurement
Anisocyte Measurement
phenotype Laboratory Procedure 15 0.100 None 0
CUI: C0020433
Disease: Hyperbilirubinemia
Hyperbilirubinemia
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 131 27 0.100 None 0
Increased lactate dehydrogenase activity
phenotype Finding 27 0.100 None 0
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
group Neoplasms Neoplastic Process 8621 1641 0.020 None 1.000 2 2006 2020
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
group Neoplasms Neoplastic Process 8221 1374 0.020 None 1.000 2 2006 2020