TPI1, triosephosphate isomerase 1, 7167

N. diseases: 184; N. variants: 10
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: C1860808
Disease: Triosephosphate Isomerase Deficiency
Triosephosphate Isomerase Deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 1 9 0.900 strong 1.000 19 9 1986 2018
CUI: C0398562
Disease: Triose phosphate isomerase deficiency
Triose phosphate isomerase deficiency 		disease Disease or Syndrome 1 0.310 None 1.000 1 2010 2010
CUI: C4016412
Disease: TRIOSEPHOSPHATE ISOMERASE MANCHESTER
TRIOSEPHOSPHATE ISOMERASE MANCHESTER 		disease Finding 1 1 0.100 None 0 1
CUI: C0752251
Disease: Muscle Disease Manifestations
Muscle Disease Manifestations 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 2 0.300 None 1.000 2 1986 1993
CUI: C0002735
Disease: Oppenheim's Disease
Oppenheim's Disease 		disease Nervous System Diseases Disease or Syndrome; Congenital Abnormality 2 0.300 None 1.000 1 1993 1993
CUI: C4505386
Disease: Giardia duodenalis Infection
Giardia duodenalis Infection 		disease Digestive System Diseases; Infections Disease or Syndrome 2 0.010 None 1.000 1 2018 2018
CUI: C4551685
Disease: Paralysis of diaphragm
Paralysis of diaphragm 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Finding 2 4 0.100 None 0 1
CUI: C0752252
Disease: Neuromuscular Manifestations
Neuromuscular Manifestations 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 3 0.300 None 1.000 2 1986 1993
CUI: C0751381
Disease: Foley-Denny-Brown Syndrome
Foley-Denny-Brown Syndrome 		disease Nervous System Diseases Disease or Syndrome 3 0.300 None 1.000 1 1993 1993
CUI: C0085407
Disease: Microsporidiosis
Microsporidiosis 		disease Infections Disease or Syndrome 4 0.010 None 1.000 1 2018 2018
CUI: C3277687
Disease: Central nervous system degeneration
Central nervous system degeneration 		phenotype Finding 4 0.100 None 0
CUI: C0002882
Disease: Anemia, Hemolytic, Congenital Nonspherocytic
Anemia, Hemolytic, Congenital Nonspherocytic 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 5 0.300 None 1.000 1 1993 1993
CUI: C3665488
Disease: Familial Osteochondritis Dissecans
Familial Osteochondritis Dissecans 		disease Musculoskeletal Diseases Disease or Syndrome 5 1 0.010 None 1.000 1 2011 2011
CUI: C0859021
Disease: Hyperthymic state
Hyperthymic state 		disease Mental or Behavioral Dysfunction 8 5 0.010 None 1.000 1 2017 2017
CUI: C0857501
Disease: Acute schizophrenia
Acute schizophrenia 		disease Mental or Behavioral Dysfunction 9 0.300 None 1.000 1 2012 2012
CUI: C0235983
Disease: Normochromic anemia
Normochromic anemia 		phenotype Hemic and Lymphatic Diseases Disease or Syndrome 9 0.100 None 0
CUI: C0085577
Disease: Normocytic anemia
Normocytic anemia 		disease Hemic and Lymphatic Diseases Disease or Syndrome 12 0.100 None 0
CUI: C0002889
Disease: Anemia, Microangiopathic
Anemia, Microangiopathic 		disease Hemic and Lymphatic Diseases Disease or Syndrome 13 0.300 None 1.000 1 1986 1986
CUI: C1276071
Disease: Childhood atopic dermatitis
Childhood atopic dermatitis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 13 0.010 None 1.000 1 2006 2006
CUI: C0035232
Disease: Respiratory Paralysis
Respiratory Paralysis 		phenotype Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Nervous System Diseases Finding 13 1 0.100 None 0
CUI: C1332629
Disease: Breast Fibrocystic Change, Proliferative Type
Breast Fibrocystic Change, Proliferative Type 		disease Skin and Connective Tissue Diseases Disease or Syndrome 14 0.010 None 1.000 1 2004 2004
CUI: C1387532
Disease: Chronic hemolytic anemia
Chronic hemolytic anemia 		disease Hemic and Lymphatic Diseases Disease or Syndrome 15 5 0.110 None 1.000 1 1978 1978
CUI: C0002879
Disease: Anemia, Hemolytic, Acquired
Anemia, Hemolytic, Acquired 		disease Hemic and Lymphatic Diseases Disease or Syndrome 16 1 0.300 None 1.000 1 1986 1986
CUI: C0520572
Disease: Enzymopathy
Enzymopathy 		group Nutritional and Metabolic Diseases Disease or Syndrome 17 1 0.330 strong 0.800 5 1 1978 2008
CUI: C0025290
Disease: Aseptic Meningitis
Aseptic Meningitis 		disease Nervous System Diseases Disease or Syndrome 17 0.010 None 1.000 1 2017 2017