Frequent falls
Symptom Information:
Symptom ID: | HPO:0002359 | ||||
Synonyms: |
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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 musculature(HPO:0003011) Abnormality of muscle physiology(HPO:0011804) Functional motor problems(HPO:0004302) Frequent falls(HPO:0002359) Abnormality of the nervous system(HPO:0000707) Abnormality of nervous system physiology(HPO:0012638) Abnormality of central motor function(HPO:0011442) Abnormality of coordination(HPO:0011443) Incoordination(HPO:0002311) Frequent falls(HPO:0002359) MedDRA: |
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Database Frequency: | 24 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
ATAXIA-OCULOMOTOR APRAXIA 3 | (OMIM:615217) |
Argininemia | (Orphanet:90) |
Ataxia-telangiectasia-like disorder | (Orphanet:251347) |
Autosomal dominant Charcot-Marie-Tooth disease type 2O | (Orphanet:284232) |
Autosomal recessive limb-girdle muscular dystrophy type 2I | (Orphanet:34515) |
Autosomal recessive spastic paraplegia type 26 | (Orphanet:101006) |
Charcot-Marie-Tooth disease type 4J | (Orphanet:139515) |
Congenital muscular dystrophy with cerebellar involvement | (Orphanet:370959) |
Congenital myopathy with excess of thin filaments | (Orphanet:98904) |
HYPEREKPLEXIA, HEREDITARY 1 | (OMIM:149400) |
Hereditary hyperekplexia | (Orphanet:3197) |
Hereditary motor and sensory neuropathy type 5 | (Orphanet:64751) |
Hereditary myoclonus - progressive distal muscular atrophy | (Orphanet:2590) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5 | (OMIM:606612) |
MYASTHENIC SYNDROME, CONGENITAL, 15 | (OMIM:616227) |
MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET | (OMIM:614399) |
MYOPATHY, REDUCING BODY, X-LINKED, CHILDHOOD-ONSET | (OMIM:300718) |
NEMALINE MYOPATHY 2 | (OMIM:256030) |
Nemaline myopathy | (Orphanet:607) |
SPASTIC ATAXIA 2, AUTOSOMAL RECESSIVE | (OMIM:611302) |
SPINOCEREBELLAR ATAXIA 37 | (OMIM:615945) |
STRIATONIGRAL DEGENERATION, INFANTILE, MITOCHONDRIAL | (OMIM:500003) |
Stiff person syndrome | (Orphanet:3198) |
Tubular aggregate myopathy | (Orphanet:2593) |