CDAN1, codanin 1, 146059

N. diseases: 46; N. variants: 12
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.
Congenital dyserythropoietic anemia, type I
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 5 11 0.750 1.000 10 11 1993 2013
CUI: C0002876
Disease: Congenital dyserythropoietic anemia
Congenital dyserythropoietic anemia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 18 4 0.380 1.000 8 1 1994 2014
CUI: C0010828
Disease: Cytopenia
Cytopenia
phenotype Pathologic Function 206 0.300 strong 1 2003 2003
CUI: C0158995
Disease: Congenital anemia
Congenital anemia
disease Disease or Syndrome 208 0.300 strong 1 2003 2003
Congenital dyserythropoietic anemia, type III
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 6 0.300 0
Congenital dyserythropoietic anemia, type II
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 15 8 0.300 0
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors
phenotype Behavior and Behavior Mechanisms Individual Behavior 208 753 0.100 1 1 2015 2015
CUI: C0038002
Disease: Splenomegaly
Splenomegaly
phenotype Pathological Conditions, Signs and Symptoms Finding 246 3 0.100 0
CUI: C0206160
Disease: Reticulocytosis
Reticulocytosis
phenotype Pathological Conditions, Signs and Symptoms Finding 25 0.100 0
CUI: C0221281
Disease: Poikilocytosis
Poikilocytosis
phenotype Finding 6 0.100 0
CUI: C0022353
Disease: Neonatal Jaundice
Neonatal Jaundice
phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Pathological Conditions, Signs and Symptoms Disease or Syndrome 34 0.100 0
CUI: C0221278
Disease: Anisocytosis
Anisocytosis
phenotype Finding 9 0.100 0
CUI: C0020305
Disease: Hydrops Fetalis
Hydrops Fetalis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Hemic and Lymphatic Diseases; Immune System Diseases; Pathological Conditions, Signs and Symptoms Disease or Syndrome 102 2 0.100 0
CUI: C1835580
Disease: Mild postnatal growth retardation
Mild postnatal growth retardation
phenotype Finding 6 0.100 0
Endopolyploidy on chromosome studies of bone marrow
phenotype Finding 2 0.100 0
CUI: C4025183
Disease: Macrocytic dyserythropoietic anemia
Macrocytic dyserythropoietic anemia
disease Disease or Syndrome 2 0.100 0
Reduced activity of N-acetylglucosaminyltransferase II
phenotype Finding 2 0.100 0
CUI: C3550204
Disease: Mild growth deficiency
Mild growth deficiency
phenotype Finding 6 0.100 0
Bone marrow smear shows erythroid hyperplasia
phenotype Finding 5 0.100 0
CUI: C1859236
Disease: Prolonged neonatal jaundice
Prolonged neonatal jaundice
phenotype Finding 24 0.100 0
Bone marrow biopsy shows erythroid hyperplasia
phenotype Laboratory or Test Result 5 0.100 0
CUI: C0014800
Disease: Erythroid hyperplasia
Erythroid hyperplasia
disease Disease or Syndrome 17 1 0.100 0
CUI: C3469186
Disease: HEMOCHROMATOSIS, TYPE 1
HEMOCHROMATOSIS, TYPE 1
disease Disease or Syndrome 64 42 0.020 1.000 2 2004 2009
CUI: C0282193
Disease: Iron Overload
Iron Overload
disease Nutritional and Metabolic Diseases Disease or Syndrome 87 30 0.020 1.000 2 2006 2007
CUI: C0015672
Disease: Fatigue
Fatigue
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 329 33 0.020 1.000 2 2016 2016