UPK3B, uroplakin 3B, 105375355

N. diseases: 82; 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: C1848199
Disease: X-Linked Lissencephaly
X-Linked Lissencephaly 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 14 1 0.010 None 1.000 1 2000 2000
CUI: C4025320
Disease: Craniofacial asymmetry
Craniofacial asymmetry 		disease Pathological Conditions, Signs and Symptoms Anatomical Abnormality 16 0.010 None 1.000 1 2017 2017
CUI: C0013589
Disease: Ectromelia
Ectromelia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Congenital Abnormality 30 0.010 None 1.000 1 2018 2018
CUI: C0037354
Disease: Smallpox
Smallpox 		disease Infections Disease or Syndrome 39 0.010 None 1.000 1 2018 2018
CUI: C0014740
Disease: Erythema Chronicum Migrans
Erythema Chronicum Migrans 		disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 41 0.010 None 1.000 1 1998 1998
CUI: C0017677
Disease: Glossitis, Benign Migratory
Glossitis, Benign Migratory 		disease Stomatognathic Diseases Disease or Syndrome 53 1 0.010 None 1.000 1 1998 1998
CUI: C0242381
Disease: Lyme Arthritis
Lyme Arthritis 		disease Infections Disease or Syndrome 57 0.010 None 1.000 1 1998 1998
CUI: C0030524
Disease: Paratuberculosis
Paratuberculosis 		disease Infections; Animal Diseases Disease or Syndrome 61 6 0.010 None 1.000 1 2000 2000
CUI: C0035920
Disease: Rubella
Rubella 		disease Infections Disease or Syndrome 82 11 0.010 None 1.000 1 2017 2017
CUI: C0206716
Disease: Ganglioglioma
Ganglioglioma 		disease Neoplasms Neoplastic Process 91 7 0.010 None 1.000 1 2004 2004
CUI: C1562113
Disease: Fleck corneal dystrophy
Fleck corneal dystrophy 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 104 12 0.010 None 1.000 1 2008 2008
CUI: C0017574
Disease: Gingivitis
Gingivitis 		disease Infections; Stomatognathic Diseases Disease or Syndrome 152 3 0.010 None 1.000 1 2008 2008
CUI: C0079745
Disease: Lymphoma, Large-Cell, Follicular
Lymphoma, Large-Cell, Follicular 		disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 153 6 0.010 None 1.000 1 2002 2002
CUI: C0750901
Disease: Alzheimer Disease, Early Onset
Alzheimer Disease, Early Onset 		disease Nervous System Diseases; Mental Disorders Disease or Syndrome 174 96 0.010 None 1.000 1 2005 2005
CUI: C0024198
Disease: Lyme Disease
Lyme Disease 		disease Infections Disease or Syndrome 178 4 0.020 None 1.000 2 1997 1998
CUI: C0026918
Disease: Mycobacterium Infections
Mycobacterium Infections 		group Infections Disease or Syndrome 183 14 0.010 None 1.000 1 2018 2018
CUI: C0085084
Disease: Motor Neuron Disease
Motor Neuron Disease 		disease Nervous System Diseases Disease or Syndrome 186 52 0.010 None 1.000 1 2004 2004
CUI: C0023281
Disease: Leishmaniasis
Leishmaniasis 		disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 198 4 0.010 None 1.000 1 2019 2019
CUI: C0220756
Disease: Niemann-Pick Disease, Type C
Niemann-Pick Disease, Type C 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 201 33 0.010 None 1.000 1 2006 2006
CUI: C0035344
Disease: Retinopathy of Prematurity
Retinopathy of Prematurity 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 202 16 0.020 None 1.000 2 2019 2020
CUI: C3665346
Disease: Unspecified visual loss
Unspecified visual loss 		phenotype Pathological Conditions, Signs and Symptoms; Eye Diseases Sign or Symptom 235 11 0.010 None 1.000 1 2005 2005
CUI: C0039483
Disease: Giant Cell Arteritis
Giant Cell Arteritis 		disease Skin and Connective Tissue Diseases; Immune System Diseases; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 260 78 0.010 None 1.000 1 2018 2018
CUI: C0276496
Disease: Familial Alzheimer Disease (FAD)
Familial Alzheimer Disease (FAD) 		disease Nervous System Diseases; Mental Disorders Disease or Syndrome 260 95 0.010 None 1.000 1 2017 2017
CUI: C0003578
Disease: Apnea
Apnea 		phenotype Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases Sign or Symptom 262 11 0.010 None 1.000 1 2018 2018
CUI: C0041341
Disease: Tuberous Sclerosis
Tuberous Sclerosis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nervous System Diseases Neoplastic Process 289 55 0.010 None 1.000 1 2012 2012