KLF1, Kruppel like factor 1, 10661

N. diseases: 64; N. variants: 15
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: C1292231
Disease: In(Lu) phenotype (finding)
In(Lu) phenotype (finding) 		phenotype Finding 1 10 0.400 moderate 0 10
CUI: C3150805
Disease: FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 6
FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 6 		phenotype Finding 1 3 0.400 moderate 0 3
CUI: C4023619
Disease: Absence of Lutheran antigen on erythrocytes
Absence of Lutheran antigen on erythrocytes 		disease Anatomical Abnormality 1 1 0.100 None 0 1
CUI: C3150926
Disease: Congenital dyserythropoietic anemia type IV
Congenital dyserythropoietic anemia type IV 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 2 6 0.780 None 1.000 10 3 2010 2020
CUI: C0221016
Disease: Red blood cell disorder
Red blood cell disorder 		group Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases Disease or Syndrome 6 0.020 None 1.000 2 2016 2019
CUI: C0002891
Disease: Anemia, Neonatal
Anemia, Neonatal 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 6 0.010 None < 0.001 1 2017 2017
CUI: C0271934
Disease: Congenital dyserythropoietic anemia, type III
Congenital dyserythropoietic anemia, type III 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 6 0.300 None 0
CUI: C4025630
Disease: Abnormal bone structure
Abnormal bone structure 		disease Anatomical Abnormality 7 0.100 None 0
CUI: C0238159
Disease: Hemoglobin E disease
Hemoglobin E disease 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 8 4 0.010 None 1.000 1 2015 2015
CUI: C0271933
Disease: Congenital dyserythropoietic anemia, type I
Congenital dyserythropoietic anemia, type I 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 8 12 0.300 None 0
CUI: C4023620
Disease: Blood group antigen abnormality
Blood group antigen abnormality 		phenotype Anatomical Abnormality 8 6 0.100 None 0 1
CUI: C0239941
Disease: Persistence of hemoglobin F
Persistence of hemoglobin F 		phenotype Finding 9 0.100 None 0
CUI: C0678199
Disease: Anemia of inadequate production
Anemia of inadequate production 		disease Hemic and Lymphatic Diseases Disease or Syndrome 10 3 0.100 None 0
CUI: C1306589
Disease: Congenital dyserythropoietic anemia, type II
Congenital dyserythropoietic anemia, type II 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 21 14 0.300 None 0
CUI: C0014800
Disease: Erythroid hyperplasia
Erythroid hyperplasia 		disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 22 3 0.100 None 0
CUI: C0002876
Disease: Congenital dyserythropoietic anemia
Congenital dyserythropoietic anemia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 24 13 0.560 strong 1.000 7 2 2010 2020
CUI: C0271901
Disease: Microcytic hypochromic anemia (disorder)
Microcytic hypochromic anemia (disorder) 		disease Hemic and Lymphatic Diseases Disease or Syndrome 25 3 0.010 None 1.000 1 2015 2015
CUI: C0019025
Disease: Hemoglobin F Disease
Hemoglobin F Disease 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 27 0.320 None 1.000 2 2010 2013
CUI: C3161174
Disease: Hemoglobin H Disease
Hemoglobin H Disease 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 29 0.010 None 1.000 1 2015 2015
CUI: C0271994
Disease: Hereditary persistence of fetal hemoglobin thalassemia
Hereditary persistence of fetal hemoglobin thalassemia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 35 0.030 None 1.000 3 2010 2017
CUI: C0206160
Disease: Reticulocytosis
Reticulocytosis 		phenotype Pathological Conditions, Signs and Symptoms Finding 40 1 0.100 None 0
CUI: C1292779
Disease: Myelodysplastic Syndrome with Isolated del(5q)
Myelodysplastic Syndrome with Isolated del(5q) 		disease Hemic and Lymphatic Diseases Neoplastic Process 41 1 0.010 None 1.000 1 2013 2013
CUI: C1802398
Disease: Chromosome 5, trisomy 5q
Chromosome 5, trisomy 5q 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 42 1 0.010 None 1.000 1 2013 2013
CUI: C0740302
Disease: 5q-syndrome
5q-syndrome 		disease Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases Disease or Syndrome 45 1 0.010 None 1.000 1 2013 2013
CUI: C0037889
Disease: Hereditary spherocytosis
Hereditary spherocytosis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 53 13 0.210 None 1.000 1 2010 2010