TNMD, tenomodulin, 64102

N. diseases: 86; N. variants: 4
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: C0333370
Disease: Sulfur granules
Sulfur granules 		phenotype Sign or Symptom 3 0.010 None 1.000 1 2018 2018
CUI: C0038475
Disease: Double structure
Double structure 		disease Congenital Abnormality 4 0.010 None 1.000 1 2017 2017
CUI: C0339968
Disease: Neonatal pneumonia
Neonatal pneumonia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Infections; Respiratory Tract Diseases Disease or Syndrome 5 0.010 None 1.000 1 2019 2019
CUI: C0276640
Disease: Transmissible mink encephalopathy
Transmissible mink encephalopathy 		disease Pathological Conditions, Signs and Symptoms; Infections; Nervous System Diseases Disease or Syndrome 6 0.050 None 1.000 5 2011 2019
CUI: C1302652
Disease: Adenoma of rectum
Adenoma of rectum 		disease Digestive System Diseases; Neoplasms Neoplastic Process 6 0.010 None 1.000 1 2019 2019
CUI: C4316985
Disease: Cerebellar edema
Cerebellar edema 		disease Nervous System Diseases Disease or Syndrome 6 0.010 None 1.000 1 2018 2018
CUI: C0007894
Disease: Cestode Infections
Cestode Infections 		group Infections Disease or Syndrome 8 0.010 None 1.000 1 2018 2018
CUI: C0155127
Disease: Familial Amyloid Polyneuropathy, Type V
Familial Amyloid Polyneuropathy, Type V 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 8 19 0.010 None 1.000 1 2020 2020
CUI: C0302361
Disease: Disease caused by Shigella sonnei
Disease caused by Shigella sonnei 		disease Digestive System Diseases; Infections Disease or Syndrome 11 0.010 None 1.000 1 2003 2003
CUI: C0002066
Disease: Alkaptonuria
Alkaptonuria 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 13 68 0.020 None 1.000 2 2012 2017
CUI: C0026706
Disease: Mucopolysaccharidosis III
Mucopolysaccharidosis III 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 17 15 0.010 None 1.000 1 2018 2018
CUI: C0043407
Disease: Yersinia infections
Yersinia infections 		group Infections Disease or Syndrome 17 0.010 None 1.000 1 2019 2019
CUI: C0004659
Disease: Bacteriuria
Bacteriuria 		phenotype Female Urogenital Diseases and Pregnancy Complications; Infections; Male Urogenital Diseases Disease or Syndrome 18 0.010 None 1.000 1 2011 2011
CUI: C0009946
Disease: Conversion disorder
Conversion disorder 		group Mental Disorders Mental or Behavioral Dysfunction 21 1 0.030 None 1.000 3 2017 2019
CUI: C0040261
Disease: Onychomycosis
Onychomycosis 		disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 27 2 0.010 None 1.000 1 2020 2020
CUI: C3828416
Disease: Radiation Damage
Radiation Damage 		disease Wounds and Injuries Disease or Syndrome 44 0.010 None 1.000 1 2019 2019
CUI: C0026703
Disease: Mucopolysaccharidoses
Mucopolysaccharidoses 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 48 7 0.010 None 1.000 1 2018 2018
CUI: C0553681
Disease: Hypofibrinogenemia
Hypofibrinogenemia 		disease Disease or Syndrome 60 14 0.010 None 1.000 1 2018 2018
CUI: C2751492
Disease: AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 74 68 0.010 None 1.000 1 1999 1999
CUI: C0860659
Disease: Aloof
Aloof 		disease Mental or Behavioral Dysfunction 81 0.010 None 1.000 1 2019 2019
CUI: C3469186
Disease: HEMOCHROMATOSIS, TYPE 1
HEMOCHROMATOSIS, TYPE 1 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 83 62 0.010 None 1.000 1 2002 2002
CUI: C0006309
Disease: Brucellosis
Brucellosis 		disease Infections Disease or Syndrome 92 30 0.010 None 1.000 1 2018 2018
CUI: C0018995
Disease: Hemochromatosis
Hemochromatosis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 93 45 0.010 None 1.000 1 2002 2002
CUI: C0026946
Disease: Mycoses
Mycoses 		group Infections Disease or Syndrome 94 2 0.010 None 1.000 1 2019 2019
CUI: C0232197
Disease: Fibrillation
Fibrillation 		disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 118 8 0.030 None 1.000 3 2017 2019