LRRC32, leucine rich repeat containing 32, 2615

N. diseases: 58; 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: C0477474
Disease: Dermatitis and eczema
Dermatitis and eczema 		disease Skin and Connective Tissue Diseases Disease or Syndrome 6 1 0.010 None 1.000 1 2011 2011
CUI: C0205822
Disease: Hibernoma
Hibernoma 		disease Neoplasms Neoplastic Process 10 0.010 None 1.000 1 2003 2003
CUI: C1848638
Disease: USHER SYNDROME, TYPE IB (disorder)
USHER SYNDROME, TYPE IB (disorder) 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 14 11 0.010 None 1.000 1 1997 1997
CUI: C1274233
Disease: T-lymphocyte immunodeficiency
T-lymphocyte immunodeficiency 		disease Immune System Diseases Disease or Syndrome 15 2 0.010 None 1.000 1 2013 2013
CUI: C0343532
Disease: Streptococcal toxic shock syndrome
Streptococcal toxic shock syndrome 		phenotype Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 16 0.010 None 1.000 1 2018 2018
CUI: C0344290
Disease: Vitreoretinal degeneration
Vitreoretinal degeneration 		disease Disease or Syndrome 20 6 0.100 None 0 1
CUI: C0238124
Disease: Necrotizing fasciitis
Necrotizing fasciitis 		disease Musculoskeletal Diseases Disease or Syndrome 24 0.010 None 1.000 1 2018 2018
CUI: C1832097
Disease: EPIDERMAL DIFFERENTIATION COMPLEX
EPIDERMAL DIFFERENTIATION COMPLEX 		disease Disease or Syndrome 38 3 0.010 None 1.000 1 2013 2013
CUI: C0019360
Disease: Herpes zoster disease
Herpes zoster disease 		group Infections Disease or Syndrome 51 10 0.100 None 1.000 1 1 2019 2019
CUI: C0339467
Disease: Proliferative retinopathy
Proliferative retinopathy 		disease Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases Disease or Syndrome 57 7 0.010 None 1.000 1 1 2019 2019
CUI: C0409952
Disease: Idiopathic osteoarthritis
Idiopathic osteoarthritis 		disease Musculoskeletal Diseases Disease or Syndrome 63 12 0.010 None 1.000 1 2008 2008
CUI: C1384584
Disease: Generalized osteoarthritis
Generalized osteoarthritis 		disease Musculoskeletal Diseases Disease or Syndrome 63 10 0.010 None 1.000 1 2008 2008
CUI: C0014335
Disease: Enteritis
Enteritis 		disease Digestive System Diseases Disease or Syndrome 85 2 0.010 None 1.000 1 2019 2019
CUI: C0079680
Disease: Lentivirus Infections
Lentivirus Infections 		group Infections Disease or Syndrome 88 0.010 None 1.000 1 2013 2013
CUI: C0018621
Disease: Hay fever
Hay fever 		disease Respiratory Tract Diseases; Immune System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 114 42 0.010 None 1.000 1 2014 2014
CUI: C4554344
Disease: IgE-mediated food allergy
IgE-mediated food allergy 		disease Immune System Diseases Disease or Syndrome 126 16 0.010 None 1.000 1 2020 2020
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis 		disease Digestive System Diseases; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 183 40 0.010 None 1.000 1 2017 2017
CUI: C2981150
Disease: Uranostaphyloschisis
Uranostaphyloschisis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Respiratory Tract Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases Congenital Abnormality 190 75 0.110 None 1.000 1 1 2019 2019
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		phenotype Immune System Diseases Pathologic Function 197 1019 0.100 None 1.000 1 1 2013 2013
CUI: C0751967
Disease: Multiple Sclerosis, Relapsing-Remitting
Multiple Sclerosis, Relapsing-Remitting 		disease Immune System Diseases; Nervous System Diseases Disease or Syndrome 206 7 0.010 None 1.000 1 2018 2018
CUI: C0040128
Disease: Thyroid Diseases
Thyroid Diseases 		group Endocrine System Diseases Disease or Syndrome 230 26 0.010 None 1.000 1 2019 2019
CUI: C1837218
Disease: Cleft palate, isolated
Cleft palate, isolated 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases Congenital Abnormality 295 70 0.010 None 1.000 1 2019 2019
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		disease Respiratory Tract Diseases; Immune System Diseases Disease or Syndrome 303 317 0.010 None 1.000 1 2019 2019
CUI: C0742343
Disease: Acute Chest Syndrome
Acute Chest Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 405 135 0.010 None 1.000 1 2014 2014
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Disease or Syndrome 478 667 0.010 None 1.000 1 2019 2019