CBLIF, cobalamin binding intrinsic factor, 2694

N. diseases: 185; N. variants: 3
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: C4021768
Disease: Abnormality of metabolism/homeostasis
Abnormality of metabolism/homeostasis 		phenotype Finding 171 5 0.100 None 0
CUI: C1963165
Disease: Malabsorption, CTCAE
Malabsorption, CTCAE 		phenotype Finding 175 0.100 None 0
CUI: C0302845
Disease: MCV - raised
MCV - raised 		phenotype Finding 12 1 0.100 None 0
CUI: C0030554
Disease: Paresthesia
Paresthesia 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 121 8 0.100 None 0
CUI: C3714745
Disease: Malabsorption
Malabsorption 		phenotype Digestive System Diseases Finding 175 3 0.100 None 0
CUI: C0020580
Disease: Hypesthesia
Hypesthesia 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Finding 33 6 0.100 None 0
CUI: C0750292
Disease: Malabsorption of Vitamin B12
Malabsorption of Vitamin B12 		phenotype Finding 3 0.100 None 0
CUI: C4021641
Disease: Absence of intrinsic factor
Absence of intrinsic factor 		phenotype Finding 1 0.100 None 0
CUI: C4021753
Disease: Abnormality of the immune system
Abnormality of the immune system 		disease Pathologic Function 34 3 0.100 None 0
CUI: C1334688
Disease: Megaloblastic erythroid hyperplasia
Megaloblastic erythroid hyperplasia 		phenotype Finding 3 0.100 None 0
CUI: C0017152
Disease: Gastritis
Gastritis 		disease Digestive System Diseases Disease or Syndrome 292 21 0.240 None 1.000 5 1975 2019
CUI: C0018834
Disease: Heartburn
Heartburn 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 139 5 0.010 None 1.000 1 1984 1984
CUI: C0024523
Disease: Malabsorption Syndrome
Malabsorption Syndrome 		group Digestive System Diseases; Nutritional and Metabolic Diseases Disease or Syndrome 239 0.140 None 1.000 4 1985 2000
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		disease Immune System Diseases; Nervous System Diseases Disease or Syndrome 1800 1022 0.060 None 1.000 6 1989 2019
CUI: C0340782
Disease: Hyperplastic lymph node
Hyperplastic lymph node 		disease Acquired Abnormality 12 0.010 None 1.000 1 1990 1990
CUI: C0206142
Disease: Eosinophilic leukemia
Eosinophilic leukemia 		disease Hemic and Lymphatic Diseases Neoplastic Process 18 2 0.010 None 1.000 1 1990 1990
CUI: C0346421
Disease: Chronic eosinophilic leukemia
Chronic eosinophilic leukemia 		disease Neoplasms; Hemic and Lymphatic Diseases Neoplastic Process 42 9 0.010 None 1.000 1 1990 1990
CUI: C1306856
Disease: Megaloblastic anemia due to inborn errors of metabolism
Megaloblastic anemia due to inborn errors of metabolism 		disease Hemic and Lymphatic Diseases Disease or Syndrome 3 0.010 None 1.000 1 1991 1991
CUI: C0016382
Disease: Flushing
Flushing 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 83 9 0.010 None 1.000 1 1995 1995
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 1883 1172 0.040 None 1.000 4 1996 2020
CUI: C0024138
Disease: Lupus Erythematosus, Discoid
Lupus Erythematosus, Discoid 		disease Skin and Connective Tissue Diseases Disease or Syndrome 552 46 0.030 None 1.000 3 1996 2018
CUI: C0409974
Disease: Lupus Erythematosus
Lupus Erythematosus 		disease Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 558 44 0.030 None 1.000 3 1996 2018
CUI: C0024131
Disease: Lupus Vulgaris
Lupus Vulgaris 		disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 526 44 0.030 None 1.000 3 1996 2018
CUI: C0343752
Disease: Acute HIV infection
Acute HIV infection 		disease Infections; Immune System Diseases Disease or Syndrome 48 0.010 None 1.000 1 1997 1997
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		group Immune System Diseases Disease or Syndrome 1758 428 0.010 None < 0.001 1 1997 1997