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 |