CYCS, cytochrome c, somatic, 54205

N. diseases: 67; 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: C2677608
Disease: Thrombocytopenia 4
Thrombocytopenia 4
disease Hemic and Lymphatic Diseases Disease or Syndrome 1 3 0.710 None 1.000 3 3 2008 2018
CUI: C1848030
Disease: Hypotonia-Cystinuria Syndrome
Hypotonia-Cystinuria Syndrome
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases; Male Urogenital Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms Disease or Syndrome 6 0.010 None 1.000 1 2013 2013
CUI: C0859021
Disease: Hyperthymic state
Hyperthymic state
disease Mental or Behavioral Dysfunction 8 5 0.010 None 1.000 1 2005 2005
CUI: C0340613
Disease: Arterial aneurysm
Arterial aneurysm
disease Cardiovascular Diseases Anatomical Abnormality 10 2 0.010 None 1.000 1 2018 2018
Posterior Circulation Transient Ischemic Attack
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 10 0.300 None 1.000 1 2001 2001
Carotid Circulation Transient Ischemic Attack
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 10 0.300 None 1.000 1 2001 2001
Transient Ischemic Attack, Vertebrobasilar Circulation
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 10 0.300 None 1.000 1 2001 2001
Crescendo Transient Ischemic Attacks
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 10 0.300 None 1.000 1 2001 2001
CUI: C0751022
Disease: Brain Stem Ischemia, Transient
Brain Stem Ischemia, Transient
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 10 0.300 None 1.000 1 2001 2001
Transient Ischemic Attack, Anterior Circulation
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 10 0.300 None 1.000 1 2001 2001
Hyperferritinemia, hereditary, with congenital cataracts
disease Nutritional and Metabolic Diseases; Eye Diseases Disease or Syndrome 10 10 0.010 None 1.000 1 2010 2010
CUI: C0010691
Disease: Cystinuria
Cystinuria
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 22 83 0.010 None 1.000 1 2013 2013
CUI: C0270971
Disease: Floppy infant syndrome
Floppy infant syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 31 6 0.010 None 1.000 1 2013 2013
CUI: C1855119
Disease: Methylmalonic aciduria
Methylmalonic aciduria
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 33 4 0.300 None 1.000 1 2006 2006
CUI: C0263454
Disease: Chloracne
Chloracne
disease Skin and Connective Tissue Diseases Disease or Syndrome 38 0.300 None 1.000 1 2007 2007
CUI: C3536715
Disease: AA amyloidosis
AA amyloidosis
disease Nutritional and Metabolic Diseases Disease or Syndrome 38 10 0.010 None 1.000 1 2012 2012
CUI: C0007965
Disease: Chediak-Higashi Syndrome
Chediak-Higashi Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 41 14 0.010 None 1.000 1 2019 2019
CUI: C0221014
Disease: Reactive systemic amyloidosis
Reactive systemic amyloidosis
disease Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 41 11 0.010 None 1.000 1 2012 2012
CUI: C0268583
Disease: Methylmalonic acidemia
Methylmalonic acidemia
phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 44 35 0.300 None 1.000 1 2006 2006
CUI: C0037285
Disease: Skin Manifestations
Skin Manifestations
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 50 5 0.010 None 1.000 1 2018 2018
CUI: C1258104
Disease: Diffuse Scleroderma
Diffuse Scleroderma
disease Skin and Connective Tissue Diseases Disease or Syndrome 56 5 0.010 None 1.000 1 2019 2019
CUI: C0005818
Disease: Blood Platelet Disorders
Blood Platelet Disorders
group Hemic and Lymphatic Diseases Disease or Syndrome 59 5 0.010 None 1.000 1 2000 2000
Cervical intraepithelial neoplasia grade 2
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications Neoplastic Process 77 3 0.010 None 1.000 1 2017 2017
CUI: C0878787
Disease: Growth failure
Growth failure
phenotype Disease or Syndrome 84 7 0.010 None 1.000 1 2013 2013
Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis
disease Immune System Diseases; Cardiovascular Diseases Disease or Syndrome 86 3 0.010 None 1.000 1 2019 2019