CD59, CD59 molecule (CD59 blood group), 966

N. diseases: 262; N. variants: 7
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: C1263777
Disease: Neoplasm of body of uterus
Neoplasm of body of uterus 		disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications Neoplastic Process 1 0.010 None 1.000 1 2015 2015
CUI: C4755276
Disease: Primary CD59 deficiency
Primary CD59 deficiency 		disease Nervous System Diseases Disease or Syndrome 1 0.300 strong 1.000 1 2015 2015
CUI: C2936826
Disease: Fumaric aciduria
Fumaric aciduria 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Behavior and Behavior Mechanisms Disease or Syndrome 2 0.010 None 1.000 1 1979 1979
CUI: C4538570
Disease: COMPLEMENT HYPERACTIVATION, ANGIOPATHIC THROMBOSIS, AND PROTEIN-LOSING ENTEROPATHY
COMPLEMENT HYPERACTIVATION, ANGIOPATHIC THROMBOSIS, AND PROTEIN-LOSING ENTEROPATHY 		disease Disease or Syndrome 3 6 0.010 None 1.000 1 2019 2019
CUI: C3872560
Disease: Acute vascular graft rejection
Acute vascular graft rejection 		disease Disease or Syndrome 4 0.020 None 1.000 2 1998 2000
CUI: C1504514
Disease: Infection by human herpesvirus 7
Infection by human herpesvirus 7 		disease Infections Disease or Syndrome 4 0.010 None 1.000 1 2007 2007
CUI: C2676767
Disease: CD59 Deficiency
CD59 Deficiency 		disease Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 5 4 0.760 None 1.000 9 3 1992 2019
CUI: C4727002
Disease: Chronic Hemolysis
Chronic Hemolysis 		disease Disease or Syndrome 6 1 0.330 strong 1.000 4 1 2015 2019
CUI: C0333227
Disease: Microembolus
Microembolus 		disease Cardiovascular Diseases Acquired Abnormality 7 0.010 None 1.000 1 2019 2019
CUI: C0019050
Disease: Hemoglobinuria, Paroxysmal
Hemoglobinuria, Paroxysmal 		disease Hemic and Lymphatic Diseases Disease or Syndrome 9 0.010 None 1.000 1 2008 2008
CUI: C4086945
Disease: Ventilatory Threshold
Ventilatory Threshold 		phenotype Sign or Symptom 10 1 0.010 None 1.000 1 2007 2007
CUI: C0457193
Disease: Soft tissue mass
Soft tissue mass 		phenotype Anatomical Abnormality 12 1 0.010 None 1.000 1 2020 2020
CUI: C1836438
Disease: Familial neurocardiogenic syncope
Familial neurocardiogenic syncope 		disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 16 1 0.010 None 1.000 1 2017 2017
CUI: C1148551
Disease: X-Linked Dyskeratosis Congenita
X-Linked Dyskeratosis Congenita 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 17 33 0.300 strong 1.000 1 2014 2014
CUI: C0037231
Disease: Sjogren-Larsson Syndrome
Sjogren-Larsson Syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 20 28 0.010 None 1.000 1 1992 1992
CUI: C4551647
Disease: Long QT Syndrome 1
Long QT Syndrome 1 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Disease or Syndrome 20 240 0.010 None 1.000 1 2002 2002
CUI: C0948242
Disease: Nuchal bleb, familial
Nuchal bleb, familial 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Immune System Diseases; Hemic and Lymphatic Diseases Congenital Abnormality 24 9 0.010 None 1.000 1 1997 1997
CUI: C1809471
Disease: Familial benign hypercalcemia
Familial benign hypercalcemia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Endocrine System Diseases Disease or Syndrome 24 35 0.010 None 1.000 1 1984 1984
CUI: C1299624
Disease: Postural Orthostatic Tachycardia Syndrome
Postural Orthostatic Tachycardia Syndrome 		disease Nervous System Diseases Disease or Syndrome 25 1 0.010 None 1.000 1 2007 2007
CUI: C1806780
Disease: Increased CSF protein
Increased CSF protein 		phenotype Finding 26 1 0.100 None 0
CUI: C0751362
Disease: Narcolepsy-Cataplexy Syndrome
Narcolepsy-Cataplexy Syndrome 		disease Nervous System Diseases; Mental Disorders Disease or Syndrome 30 7 0.010 None 1.000 1 2010 2010
CUI: C0027814
Disease: Neuritis, Autoimmune, Experimental
Neuritis, Autoimmune, Experimental 		disease Immune System Diseases; Nervous System Diseases Experimental Model of Disease 32 0.200 None 1.000 1 1999 1999
CUI: C2939094
Disease: Skin sensitisation
Skin sensitisation 		disease Disease or Syndrome 34 0.010 None 1.000 1 2019 2019
CUI: C0235574
Disease: Intravascular hemolysis
Intravascular hemolysis 		disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 36 0.060 None 1.000 6 1996 2018
CUI: C1848934
Disease: SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME
SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 36 19 0.010 None 1.000 1 2012 2012