Source: CURATED

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes Num. SNPs
C0036341 Schizophrenia disease Mental Disorders Mental or Behavioral Dysfunction disease of mental health Abnormality of the nervous system 883 1629
C0376358 Malignant neoplasm of prostate disease Neoplasms; Male Urogenital Diseases Neoplastic Process disease of anatomical entity; disease of cellular proliferation Abnormality of the genitourinary system 616 281
C0033578 Prostatic Neoplasms group Neoplasms; Male Urogenital Diseases Neoplastic Process disease of anatomical entity; disease of cellular proliferation Abnormality of the genitourinary system 616 1
C0029408 Degenerative polyarthritis disease Musculoskeletal Diseases Disease or Syndrome disease of anatomical entity Abnormality of the skeletal system 93 76
C0086743 Osteoarthrosis Deformans disease Musculoskeletal Diseases Disease or Syndrome 93 0
C0242422 Parkinsonian Disorders group Nervous System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the nervous system 30 6
C0752105 Parkinsonism, Juvenile disease Nervous System Diseases Disease or Syndrome 30 0
C1868675 PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE disease Nervous System Diseases Disease or Syndrome genetic disease; disease of anatomical entity 28 29
C0242423 Ramsay Hunt Paralysis Syndrome disease Nervous System Diseases Disease or Syndrome 28 0
C0752097 Autosomal Dominant Juvenile Parkinson Disease disease Nervous System Diseases Disease or Syndrome 28 0
C0752098 Autosomal Dominant Parkinsonism disease Nervous System Diseases Disease or Syndrome 28 0
C0752100 Autosomal Recessive Parkinsonism disease Nervous System Diseases Disease or Syndrome 28 0
C0752101 Parkinsonism, Experimental disease Nervous System Diseases Experimental Model of Disease 28 0
C0752104 Familial Juvenile Parkinsonism disease Nervous System Diseases Disease or Syndrome 28 0
C0025312 Meningomyelocele disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Congenital Abnormality disease of anatomical entity; physical disorder Abnormality of the nervous system 4 4
C0086664 Myelocele disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Congenital Abnormality disease of anatomical entity; physical disorder 4 1
C0751316 Acquired Meningomyelocele phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Acquired Abnormality disease of anatomical entity; physical disorder 4 0