Falls
Symptom Information:
Symptom ID: | HPO:0002527 | ||||
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) Falls(HPO:0002527) MedDRA: Injury, poisoning and procedural complications(MedDRA:10022117) Injuries NEC(MedDRA:10022114) Non-site specific injuries NEC(MedDRA:10029511) Falls(HPO:0002527) |
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Database Frequency: | 10 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Autosomal recessive spastic ataxia of Charlevoix-Saguenay | (Orphanet:98) |
Autosomal recessive spastic paraplegia type 11 | (Orphanet:2822) |
Autosomal recessive spastic paraplegia type 48 | (Orphanet:306511) |
Classical progressive supranuclear palsy | (Orphanet:240071) |
Duchenne muscular dystrophy | (Orphanet:98896) |
Familial cortical myoclonus | (Orphanet:319189) |
Leber congenital amaurosis 14 | (OMIM:613341) |
SUPRANUCLEAR PALSY, PROGRESSIVE, 1 | (OMIM:601104) |
SUPRANUCLEAR PALSY, PROGRESSIVE, 2 | (OMIM:609454) |
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers | (Orphanet:206546) |