CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes Num. SNPs
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
C0029408 Degenerative polyarthritis disease Musculoskeletal Diseases Disease or Syndrome disease of anatomical entity Abnormality of the skeletal system 93 76
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
C0036341 Schizophrenia disease Mental Disorders Mental or Behavioral Dysfunction disease of mental health Abnormality of the nervous system 883 1629
C0086664 Myelocele disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Congenital Abnormality disease of anatomical entity; physical disorder 4 1
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
C0242423 Ramsay Hunt Paralysis Syndrome disease Nervous System Diseases Disease or Syndrome 28 0
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
C0751316 Acquired Meningomyelocele phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Acquired Abnormality disease of anatomical entity; physical disorder 4 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
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