Source: ALL

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes Num. SNPs
C0023893 Liver Cirrhosis, Experimental disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases Experimental Model of Disease 870 0
C1963184 Nystagmus, CTCAE 3.0 phenotype Finding 779 0
C4554036 Nystagmus, CTCAE 5.0 phenotype Finding 779 0
C3714514 Infection group Infections Pathologic Function 491 0
C4553743 Spasticity, CTCAE phenotype Finding 477 0
C3665347 Visual Impairment phenotype Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Finding Abnormality of the eye 422 0
C1531647 Cerebral ventriculomegaly phenotype Nervous System Diseases Finding disease of anatomical entity 410 0
C0039103 Synovitis disease Musculoskeletal Diseases Disease or Syndrome disease of anatomical entity Abnormality of the skeletal system 197 0
C0012546 Diphtheria disease Infections Disease or Syndrome 147 0
C4552810 Irritability, CTCAE phenotype Finding 140 0
C0751494 Convulsive Seizures phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 117 0
C4553765 Memory Impairment, CTCAE 5.0 phenotype Finding 108 0
C1258666 Myxoid cyst disease Neoplasms; Skin and Connective Tissue Diseases Disease or Syndrome 106 0
C0546126 Acute Confusional Senile Dementia disease Nervous System Diseases; Mental Disorders Mental or Behavioral Dysfunction 99 0
C0750900 Alzheimer's Disease, Focal Onset disease Nervous System Diseases; Mental Disorders Mental or Behavioral Dysfunction 99 0
C0027659 Neoplasms, Experimental phenotype Neoplasms Neoplastic Process; Experimental Model of Disease 95 0
C0751781 Dentatorubral-Pallidoluysian Atrophy disease Nervous System Diseases Disease or Syndrome genetic disease; disease of anatomical entity 95 0
C0085648 Synovial Cyst disease Neoplasms Disease or Syndrome 87 0
C0860659 Aloof disease Mental or Behavioral Dysfunction 81 0
C0027540 Necrosis phenotype Pathological Conditions, Signs and Symptoms Organ or Tissue Function 60 0
C0262404 Cerebellar degeneration disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome Abnormality of the nervous system 60 0
C1837352 Childhood onset phenotype Finding 56 0
C3711376 Isodicentric Chromosome 15 Syndrome disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Disease or Syndrome 39 0
C1838681 Rapidly progressive phenotype Finding 38 0
C1850496 Neuronal loss in central nervous system phenotype Finding Abnormality of the nervous system 37 0