Frequent falls

Symptom Information:

Symptom ID: HPO:0002359
Synonyms:
Frequent falls [OMIM:Frequent falls]
Frequent falling [OMIM:Frequent falling]
Quality:
Cross references:
OMIM: "Frequent falls" [OMIM:Frequent falls]
OMIM: "Frequent falling" [OMIM:Frequent falling]
Is a (Direct Parents):
HPO         Incoordination
HPO         Functional motor problems
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 central motor function(HPO:0011442)
                Abnormality of coordination(HPO:0011443)
                   Incoordination(HPO:0002311)
                      Frequent falls(HPO:0002359)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of muscle physiology(HPO:0011804)
             Functional motor problems(HPO:0004302)
                Frequent falls(HPO:0002359)
MedDRA:
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)