| CUI | Disease | Vocabulary | Name in Vocabulary | Code |
|---|---|---|---|---|
| C0242422 | Parkinsonian Disorders | DO | secondary Parkinson disease | 13548 |
| C0242422 | Parkinsonian Disorders | HPO | Parkinsonism | HP:0001300 |
| C0242422 | Parkinsonian Disorders | HPO | Parkinsonian disease | HP:0001300 |
| C0242422 | Parkinsonian Disorders | MONDO | parkinsonian disorder | 0021095 |
| C0242422 | Parkinsonian Disorders | MSH | Parkinsonian Disorders | D020734 |
| C0242422 | Parkinsonian Disorders | MSH | Ramsay Hunt Paralysis Syndrome | D020734 |
| C0242422 | Parkinsonian Disorders | MSH | Autosomal Dominant Juvenile Parkinson Disease | D020734 |
| C0242422 | Parkinsonian Disorders | MSH | Autosomal Dominant Parkinsonism | D020734 |
| C0242422 | Parkinsonian Disorders | MSH | Autosomal Recessive Parkinsonism | D020734 |
| C0242422 | Parkinsonian Disorders | MSH | Parkinsonism, Experimental | D020734 |
| C0242422 | Parkinsonian Disorders | MSH | Familial Juvenile Parkinsonism | D020734 |
| C0242422 | Parkinsonian Disorders | MSH | Parkinsonism, Juvenile | D020734 |
| C0242422 | Parkinsonian Disorders | MSH | Parkinson Disease 2, Autosomal Recessive Juvenile | D020734 |
| C0242422 | Parkinsonian Disorders | NCI | Parkinsonism | C116922 |
| C0242422 | Parkinsonian Disorders | NCI | Parkinsonian Symptoms | C116922 |
| C0242422 | Parkinsonian Disorders | ORDO | Rare parkinsonian disorder | 68402 |