G6PD, glucose-6-phosphate dehydrogenase, 2539

N. diseases: 410; N. variants: 66
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: C0000737
Disease: Abdominal Pain
Abdominal Pain
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 302 18 0.100 None 0
CUI: C0221281
Disease: Poikilocytosis
Poikilocytosis
phenotype Finding 14 0.100 None 0
CUI: C0023518
Disease: Leukocytosis
Leukocytosis
phenotype Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases Disease or Syndrome 168 4 0.100 None 0
CUI: C0015967
Disease: Fever
Fever
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 1021 66 0.100 None 0
CUI: C4016522
Disease: G6PD TOMAH PHENOTYPE
G6PD TOMAH PHENOTYPE
phenotype Finding 1 1 0.100 None 0 1
CUI: C2697573
Disease: Heinz-Ehrlich Body Measurement
Heinz-Ehrlich Body Measurement
phenotype Laboratory Procedure 6 0.100 None 0
CUI: C2698117
Disease: Anisocyte Measurement
Anisocyte Measurement
phenotype Laboratory Procedure 15 0.100 None 0
CUI: C1845977
Disease: X- linked recessive
X- linked recessive
phenotype Finding 172 1 0.100 None 0
CUI: C4021648
Disease: Fava bean-induced hemolytic anemia
Fava bean-induced hemolytic anemia
disease Hemic and Lymphatic Diseases Disease or Syndrome 2 0.100 None 0
CUI: C0221278
Disease: Anisocytosis
Anisocytosis
phenotype Finding 16 1 0.100 None 0
CUI: C1847879
Disease: X-linked dominant inheritance
X-linked dominant inheritance
phenotype Finding 65 0.100 None 0
CUI: C0206160
Disease: Reticulocytosis
Reticulocytosis
phenotype Pathological Conditions, Signs and Symptoms Finding 40 1 0.100 None 0
CUI: C0030232
Disease: Pallor
Pallor
phenotype Pathological Conditions, Signs and Symptoms Finding 124 4 0.100 None 0
CUI: C0553699
Disease: Heinz body observation
Heinz body observation
phenotype Laboratory or Test Result 6 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: C0019048
Disease: Hemoglobinuria
Hemoglobinuria
disease Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Finding 8 0.100 None 0
Autosomal Recessive Chronic Granulomatous Disease
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 7 0.300 None 1.000 1 1973 1973
CUI: C0031306
Disease: Phagocyte Bactericidal Dysfunction
Phagocyte Bactericidal Dysfunction
disease Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 7 0.300 None 1.000 1 1973 1973
CUI: C0009663
Disease: Condylomata Acuminata
Condylomata Acuminata
disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 73 0.010 None 1.000 1 1976 1976
CUI: C0206693
Disease: Medullary carcinoma
Medullary carcinoma
disease Neoplasms Neoplastic Process 81 2 0.010 None 1.000 1 1976 1976
CUI: C4551683
Disease: Adrenal Gland Pheochromocytoma
Adrenal Gland Pheochromocytoma
disease Neoplasms; Endocrine System Diseases Neoplastic Process 416 50 0.010 None 1.000 1 1976 1976
CUI: C0238462
Disease: Medullary carcinoma of thyroid
Medullary carcinoma of thyroid
disease Neoplasms; Endocrine System Diseases Neoplastic Process 330 71 0.010 None 1.000 1 1976 1976
CUI: C0341047
Disease: Hypertrophy of parotid gland
Hypertrophy of parotid gland
disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Stomatognathic Diseases Disease or Syndrome 7 0.010 None 1.000 1 1976 1976
CUI: C0031511
Disease: Pheochromocytoma
Pheochromocytoma
disease Neoplasms Neoplastic Process 344 186 0.010 None 1.000 1 1976 1976
CUI: C0032461
Disease: Polycythemia
Polycythemia
disease Hemic and Lymphatic Diseases Disease or Syndrome 82 22 0.010 None 1.000 1 1976 1976