CHP1, calcineurin like EF-hand protein 1, 11261

N. diseases: 141; 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: C0850705
Disease: Adult Acquired Toxoplasmosis
Adult Acquired Toxoplasmosis 		disease Infections Disease or Syndrome 4 0.010 None 1.000 1 2017 2017
CUI: C0795825
Disease: Chromosome 8, trisomy 8p
Chromosome 8, trisomy 8p 		disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 5 0.010 None 1.000 1 1998 1998
CUI: C1858427
Disease: Limited extraocular movements
Limited extraocular movements 		phenotype Finding 11 1 0.100 None 0
CUI: C1332216
Disease: Adult Systemic Anaplastic Large Cell Lymphoma
Adult Systemic Anaplastic Large Cell Lymphoma 		disease Neoplastic Process 12 0.010 None 1.000 1 2018 2018
CUI: C1841984
Disease: GLOMUVENOUS MALFORMATIONS
GLOMUVENOUS MALFORMATIONS 		disease Neoplasms Disease or Syndrome 13 3 0.010 None 1.000 1 2007 2007
CUI: C1336548
Disease: Systemic Anaplastic Large Cell Lymphoma
Systemic Anaplastic Large Cell Lymphoma 		disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 19 0.010 None 1.000 1 2018 2018
CUI: C0006023
Disease: Borna Disease
Borna Disease 		disease Infections; Animal Diseases Disease or Syndrome 26 0.030 None 1.000 3 1998 2006
CUI: C0343751
Disease: Asymptomatic human immunodeficiency virus infection
Asymptomatic human immunodeficiency virus infection 		disease Infections; Immune System Diseases Disease or Syndrome 26 0.010 None 1.000 1 1996 1996
CUI: C4048305
Disease: Neuroepithelioma
Neuroepithelioma 		disease Neoplastic Process 28 0.020 None 1.000 2 1997 2003
CUI: C1321329
Disease: Slowed saccades
Slowed saccades 		phenotype Finding 29 4 0.100 None 0
CUI: C0281710
Disease: Childhood Large Cell Lymphoma
Childhood Large Cell Lymphoma 		disease Neoplastic Process 30 0.010 None 1.000 1 1994 1994
CUI: C4087436
Disease: HIV viraemia
HIV viraemia 		disease Infections Disease or Syndrome 32 0.010 None 1.000 1 1998 1998
CUI: C1142553
Disease: Primary HIV infection
Primary HIV infection 		disease Infections; Immune System Diseases Disease or Syndrome 38 1 0.010 None 1.000 1 2002 2002
CUI: C0747256
Disease: Parasitic infection
Parasitic infection 		group Pathological Conditions, Signs and Symptoms; 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 1994 1994
CUI: C0276548
Disease: HIV encephalitis
HIV encephalitis 		disease Infections; Immune System Diseases; Nervous System Diseases; Mental Disorders Disease or Syndrome 43 0.020 None 1.000 2 1998 2013
CUI: C0349637
Disease: Common acute lymphoblastic leukemia
Common acute lymphoblastic leukemia 		disease Neoplastic Process 43 0.010 None 1.000 1 1986 1986
CUI: C0206019
Disease: HIV Encephalopathy
HIV Encephalopathy 		disease Infections; Immune System Diseases; Nervous System Diseases; Mental Disorders Disease or Syndrome 45 0.020 None 1.000 2 1998 2013
CUI: C1136179
Disease: Hammer Toe
Hammer Toe 		phenotype Musculoskeletal Diseases Anatomical Abnormality 46 11 0.100 None 0
CUI: C0029423
Disease: Cartilaginous exostosis
Cartilaginous exostosis 		disease Neoplasms; Musculoskeletal Diseases Neoplastic Process 47 2 0.010 None 1.000 1 2002 2002
CUI: C0343752
Disease: Acute HIV infection
Acute HIV infection 		disease Infections; Immune System Diseases Disease or Syndrome 48 0.040 None 1.000 4 2011 2017
CUI: C0853112
Disease: Chronic infection with HIV
Chronic infection with HIV 		disease Disease or Syndrome 48 0.010 None 1.000 1 2004 2004
CUI: C1567741
Disease: Alport Syndrome
Alport Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases; Male Urogenital Diseases Disease or Syndrome 51 314 0.010 None 1.000 1 2003 2003
CUI: C0221232
Disease: Welts
Welts 		phenotype Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases; Immune System Diseases Sign or Symptom 53 0.020 None 1.000 2 2004 2013
CUI: C0017677
Disease: Glossitis, Benign Migratory
Glossitis, Benign Migratory 		disease Stomatognathic Diseases Disease or Syndrome 53 1 0.010 None 1.000 1 1994 1994