TAT, tyrosine aminotransferase, 6898

N. diseases: 230; N. variants: 28
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: C4020911
Disease: Herpetiform corneal ulceration
Herpetiform corneal ulceration 		disease Infections; Eye Diseases Disease or Syndrome 1 0.100 None 0
CUI: C4525218
Disease: Chicken Hepatoma
Chicken Hepatoma 		disease Neoplastic Process 2 0.010 None 1.000 1 1997 1997
CUI: C1848678
Disease: 4-Hydroxyphenylpyruvic aciduria
4-Hydroxyphenylpyruvic aciduria 		phenotype Finding 2 0.100 None 0
CUI: C0268125
Disease: Purine-nucleoside phosphorylase deficiency
Purine-nucleoside phosphorylase deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases Disease or Syndrome 4 10 0.010 None 1.000 1 2006 2006
CUI: C0268623
Disease: Tyrosinemia, Type III
Tyrosinemia, Type III 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 4 6 0.300 None 0
CUI: C0024439
Disease: Macular corneal dystrophy
Macular corneal dystrophy 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 5 2 0.010 None 1.000 1 2000 2000
CUI: C0268487
Disease: Tyrosine Transaminase Deficiency Disease
Tyrosine Transaminase Deficiency Disease 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 7 18 0.800 definitive 1.000 20 18 1969 2019
CUI: C1328440
Disease: Abnormality of amino acid metabolism
Abnormality of amino acid metabolism 		phenotype Finding 8 0.100 None 0
CUI: C0398739
Disease: Congenital disorder of glycosylation, type 2C
Congenital disorder of glycosylation, type 2C 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 9 6 0.010 None 1.000 1 2006 2006
CUI: C1785148
Disease: RAPP-HODGKIN SYNDROME
RAPP-HODGKIN SYNDROME 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Stomatognathic Diseases Disease or Syndrome 9 3 0.010 None 1.000 1 2006 2006
CUI: C1405854
Disease: Retinitis punctata albescens (disorder)
Retinitis punctata albescens (disorder) 		disease Eye Diseases Disease or Syndrome 10 10 0.010 None 1.000 1 2006 2006
CUI: C1879362
Disease: Hypertyrosinemia
Hypertyrosinemia 		disease Disease or Syndrome 13 2 0.020 None 1.000 2 1984 2006
CUI: C1456624
Disease: Methamphetamine abuse
Methamphetamine abuse 		disease Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 15 4 0.010 None 1.000 1 2017 2017
CUI: C2076596
Disease: Influenza A (H5N1)
Influenza A (H5N1) 		disease Disease or Syndrome 15 0.010 None 1.000 1 2017 2017
CUI: C0268483
Disease: Tyrosinemias
Tyrosinemias 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 17 3 0.420 None 1.000 2 1984 2006
CUI: C1865868
Disease: ALZHEIMER DISEASE 5
ALZHEIMER DISEASE 5 		disease Nervous System Diseases; Mental Disorders Disease or Syndrome 18 0.010 None 1.000 1 2011 2011
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 18 56 0.300 None 0
CUI: C0276096
Disease: Mastitis-metritis-agalactia syndrome
Mastitis-metritis-agalactia syndrome 		disease Female Urogenital Diseases and Pregnancy Complications; Infections; Skin and Connective Tissue Diseases Disease or Syndrome 23 3 0.010 None 1.000 1 2018 2018
CUI: C0272375
Disease: Antithrombin III Deficiency
Antithrombin III Deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 27 52 0.010 None 1.000 1 1997 1997
CUI: C0154575
Disease: Rumination Disorders
Rumination Disorders 		group Mental Disorders Mental or Behavioral Dysfunction 33 13 0.010 None 1.000 1 2018 2018
CUI: C0022596
Disease: Palmoplantar Keratosis
Palmoplantar Keratosis 		disease Skin and Connective Tissue Diseases; Musculoskeletal Diseases Disease or Syndrome 39 6 0.300 strong 0
CUI: C0024517
Disease: Major depression, single episode
Major depression, single episode 		disease Mental Disorders Mental or Behavioral Dysfunction 42 14 0.010 None 1.000 1 2011 2011
CUI: C0001849
Disease: AIDS Dementia Complex
AIDS Dementia Complex 		disease Infections; Immune System Diseases; Nervous System Diseases; Mental Disorders Disease or Syndrome 45 4 0.010 None 1.000 1 2014 2014
CUI: C0078911
Disease: AIDS-Associated Nephropathy
AIDS-Associated Nephropathy 		disease Female Urogenital Diseases and Pregnancy Complications; Infections; Male Urogenital Diseases; Immune System Diseases Disease or Syndrome 45 1 0.010 None 1.000 1 1999 1999
CUI: C4316812
Disease: Fibrinogen Deficiency
Fibrinogen Deficiency 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 56 4 0.010 None 1.000 1 1998 1998