Shuffling gait
Symptom Information:
Symptom ID: | HPO:0002362 | ||
Synonyms: |
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Quality: | |||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the nervous system(HPO:0000707) Abnormality of nervous system physiology(HPO:0012638) Abnormality of movement(HPO:0100022) Gait disturbance(HPO:0001288) Shuffling gait(HPO:0002362) MedDRA: |
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Database Frequency: | 13 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia | (Orphanet:313808) |
Autosomal recessive spastic paraplegia type 48 | (Orphanet:306511) |
Early-onset parkinsonism - intellectual deficit | (Orphanet:2379) |
Intellectual deficit, X-linked - psychosis - macroorchidism | (Orphanet:3077) |
Juvenile parkinsonism with intellectual deficit due to DNAJC6 deficiency | (Orphanet:352497) |
L1 syndrome | (Orphanet:275543) |
MASA syndrome | (Orphanet:2466) |
PARKINSON DISEASE 20, EARLY-ONSET | (OMIM:615530) |
PARKINSON DISEASE, LATE-ONSET | (OMIM:168600) |
Syndromic X-linked intellectual deficit due to JARID1C mutation | (Orphanet:85279) |
X-linked complicated spastic paraplegia type 1 | (Orphanet:306617) |
X-linked spastic paraplegia type 16 | (Orphanet:100997) |
Young adult-onset Parkinsonism | (Orphanet:2828) |