CDSN, corneodesmosin, 1041

N. diseases: 101; N. variants: 46
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: C1175175
Disease: Severe Acute Respiratory Syndrome
Severe Acute Respiratory Syndrome
disease Infections; Respiratory Tract Diseases Disease or Syndrome 117 1 0.100 None 1.000 27 2003 2018
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
disease Digestive System Diseases; Infections Disease or Syndrome 1449 519 0.100 None 1.000 16 1992 2019
CUI: C3694279
Disease: Middle East Respiratory Syndrome
Middle East Respiratory Syndrome
disease Infections Disease or Syndrome 53 0.100 None 1.000 12 2013 2019
CUI: C0042769
Disease: Virus Diseases
Virus Diseases
group Infections Disease or Syndrome 1471 42 0.090 None 1.000 9 2002 2018
CUI: C0263361
Disease: Psoriasis vulgaris
Psoriasis vulgaris
disease Skin and Connective Tissue Diseases Disease or Syndrome 255 80 0.060 None 0.833 6 1999 2006
CUI: C4523989
Disease: Occult hepatitis B
Occult hepatitis B
disease Disease or Syndrome 14 0.040 None 0.750 4 2013 2017
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
disease Digestive System Diseases; Infections Disease or Syndrome 1768 347 0.030 None 1.000 3 2010 2018
ENCEPHALITIS/ENCEPHALOPATHY, MILD, WITH REVERSIBLE MYELIN VACUOLIZATION
disease Disease or Syndrome 9 1 0.030 None 1.000 3 2017 2019
CUI: C0019159
Disease: Hepatitis A
Hepatitis A
disease Digestive System Diseases; Infections Disease or Syndrome 451 27 0.020 None 1.000 2 1996 2008
CUI: C0027651
Disease: Neoplasms
Neoplasms
group Neoplasms Neoplastic Process 10161 1644 0.020 None 1.000 2 2010 2019
CUI: C0023264
Disease: Leigh Disease
Leigh Disease
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 144 114 0.020 None 1.000 2 2012 2016
CUI: C0277527
Disease: Epidemic diarrhea
Epidemic diarrhea
disease Digestive System Diseases; Infections Disease or Syndrome 19 0.020 None 1.000 2 2017 2018
CUI: C0334070
Disease: Maturation defect
Maturation defect
phenotype Acquired Abnormality 43 2 0.010 None 1.000 1 2018 2018
CUI: C0311370
Disease: Lupus anticoagulant disorder
Lupus anticoagulant disorder
disease Pathological Conditions, Signs and Symptoms; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 66 14 0.010 None 1.000 1 2002 2002
CUI: C0282687
Disease: Hemorrhagic Fever, Ebola
Hemorrhagic Fever, Ebola
disease Infections Disease or Syndrome 164 1 0.010 None 1.000 1 2018 2018
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
group Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 2780 385 0.010 None 1.000 1 2011 2011
CUI: C0085620
Disease: Flaccid paralysis
Flaccid paralysis
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 4 0.010 None 1.000 1 2014 2014
CUI: C0149871
Disease: Deep Vein Thrombosis
Deep Vein Thrombosis
disease Cardiovascular Diseases Disease or Syndrome 230 93 0.010 None 1.000 1 2013 2013
CUI: C0280474
Disease: Childhood Glioblastoma
Childhood Glioblastoma
disease Neoplasms Neoplastic Process 2527 98 0.010 None 1.000 1 2015 2015
CUI: C0278878
Disease: Adult Glioblastoma
Adult Glioblastoma
disease Neoplasms Neoplastic Process 2528 98 0.010 None 1.000 1 2015 2015
CUI: C0266929
Disease: Chronic Periodontitis
Chronic Periodontitis
disease Stomatognathic Diseases Disease or Syndrome 287 99 0.010 None 1.000 1 1996 1996
CUI: C0155490
Disease: Middle Ear Cholesteatoma
Middle Ear Cholesteatoma
disease Skin and Connective Tissue Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 29 0.010 None 1.000 1 2017 2017
CUI: C0206750
Disease: Coronavirus Infections
Coronavirus Infections
group Infections Disease or Syndrome 33 0.010 None 1.000 1 2020 2020
CUI: C0265962
Disease: Ichthyosis linearis circumflexa
Ichthyosis linearis circumflexa
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome; Congenital Abnormality 64 20 0.010 None 1.000 1 2011 2011
CUI: C1853354
Disease: Peeling skin syndrome, acral type
Peeling skin syndrome, acral type
disease Skin and Connective Tissue Diseases Disease or Syndrome 4 7 0.010 None 1.000 1 2012 2012