Inability to walk
Symptom Information:
Symptom ID: | HPO:0002540 | ||||
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) Inability to walk(HPO:0002540) MedDRA: Nervous system disorders(MedDRA:10029205) Neurological disorders NEC(MedDRA:10029305) Neurological signs and symptoms NEC(MedDRA:10029306) Inability to walk(HPO:0002540) |
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Database Frequency: | 19 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
14q11.2 microdeletion syndrome | (Orphanet:261120) |
5q14.3 microdeletion syndrome | (Orphanet:228384) |
ATONIC-ASTATIC SYNDROME OF FOERSTER | (OMIM:209100) |
Adenylosuccinate lyase deficiency | (Orphanet:46) |
Allan-Herndon-Dudley syndrome | (Orphanet:59) |
Atypical Rett syndrome | (Orphanet:3095) |
Biotin-responsive basal ganglia disease | (Orphanet:65284) |
CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME4 | (OMIM:615268) |
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 4 | (OMIM:615716) |
Hurler syndrome | (Orphanet:93473) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 9 | (OMIM:614255) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 1 | (OMIM:613155) |
MYASTHENIC SYNDROME, CONGENITAL, 3A, SLOW-CHANNEL | (OMIM:616321) |
Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria | (Orphanet:1933) |
Mitochondrial DNA depletion syndrome, myopathic form | (Orphanet:254875) |
Primary Fanconi syndrome | (Orphanet:3337) |
SPASTIC PARAPLEGIA 61, AUTOSOMAL RECESSIVE | (OMIM:615685) |
Salla disease | (Orphanet:309334) |
Thiamine-responsive encephalopathy | (Orphanet:199348) |