Postural instability
Symptom Information:
| Symptom ID: | HPO:0002172 | ||
| Synonyms: |
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| Quality: | |||
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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) Postural instability(HPO:0002172) MedDRA: |
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| Database Frequency: | 22 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| 6-pyruvoyl-tetrahydropterin synthase deficiency | (Orphanet:13) |
| Adult-onset dystonia-parkinsonism | (Orphanet:199351) |
| Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia | (Orphanet:313808) |
| BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1 | (OMIM:213600) |
| Bilateral striopallidodentate calcinosis | (Orphanet:1980) |
| Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome | (Orphanet:309854) |
| Juvenile parkinsonism with intellectual deficit due to DNAJC6 deficiency | (Orphanet:352497) |
| Kufor-Rakeb syndrome | (Orphanet:306674) |
| Multiple system atrophy | (Orphanet:102) |
| PARKINSON DISEASE 11, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO | (OMIM:607688) |
| PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE EARLY-ONSET | (OMIM:260300) |
| PARKINSON DISEASE 17 | (OMIM:614203) |
| PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE | (OMIM:600116) |
| PARKINSON DISEASE 20, EARLY-ONSET | (OMIM:615530) |
| PARKINSON DISEASE 6, AUTOSOMAL RECESSIVE EARLY-ONSET | (OMIM:605909) |
| PARKINSON DISEASE 8, AUTOSOMAL DOMINANT | (OMIM:607060) |
| PARKINSON DISEASE, LATE-ONSET | (OMIM:168600) |
| Parkinsonim due to ATP13A2 deficiency | (Orphanet:314632) |
| Rapid-onset dystonia-parkinsonism | (Orphanet:71517) |
| Spinocerebellar ataxia type 2 | (Orphanet:98756) |
| Spinocerebellar ataxia type 3 | (Orphanet:98757) |
| Young adult-onset Parkinsonism | (Orphanet:2828) |