CUI | Disease | Vocabulary | Name in Vocabulary | Code |
---|---|---|---|---|
C0030567 | Parkinson Disease | DO | Parkinson's disease 19A | 0060891 |
C0030567 | Parkinson Disease | DO | Parkinson's disease 4 | 0060895 |
C0030567 | Parkinson Disease | DO | Parkinson's disease 23 | 0060896 |
C0030567 | Parkinson Disease | DO | Parkinson's disease | 14330 |
C0030567 | Parkinson Disease | EFO | Parkinson's disease | 0002508 |
C0030567 | Parkinson Disease | ICD10 | Parkinson's disease | G20 |
C0030567 | Parkinson Disease | ICD10CM | Paralysis agitans | G20 |
C0030567 | Parkinson Disease | ICD10CM | Parkinson's disease | G20 |
C0030567 | Parkinson Disease | ICD10CM | Parkinsonism or Parkinson's disease NOS | G20 |
C0030567 | Parkinson Disease | ICD10CM | Idiopathic Parkinsonism or Parkinson's disease | G20 |
C0030567 | Parkinson Disease | ICD10CM | Primary Parkinsonism or Parkinson's disease | G20 |
C0030567 | Parkinson Disease | ICD10CM | Hemiparkinsonism | G20 |
C0030567 | Parkinson Disease | ICD9CM | Parkinson's disease | 332 |
C0030567 | Parkinson Disease | ICD9CM | Paralysis agitans | 332.0 |
C0030567 | Parkinson Disease | MONDO | Parkinson disease | 0005180 |
C0030567 | Parkinson Disease | MONDO | autosomal dominant Parkinson disease 4 | 0011562 |
C0030567 | Parkinson Disease | MONDO | juvenile onset Parkinson disease 19A | 0014231 |
C0030567 | Parkinson Disease | MONDO | autosomal recessive early-onset Parksinson disease 23 | 0014796 |
C0030567 | Parkinson Disease | MSH | Parkinson Disease | D010300 |
C0030567 | Parkinson Disease | NCI | Parkinson's Disease | C26845 |
C0030567 | Parkinson Disease | NCI | Parkinson Disease | C26845 |
C0030567 | Parkinson Disease | NCI | Anemia | OMFAQ |
C0030567 | Parkinson Disease | NCI | Arthritis | OMFAQ |
C0030567 | Parkinson Disease | NCI | Asthma | OMFAQ |
C0030567 | Parkinson Disease | NCI | Cerebral Palsy | OMFAQ |