Apraxia
Symptom Information:
Symptom ID: | HPO:0002186 | |||||||||||||||
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 nervous system(HPO:0000707) Abnormality of nervous system physiology(HPO:0012638) Abnormality of higher mental function(HPO:0011446) Apraxia(HPO:0002186) Abnormality of central motor function(HPO:0011442) Apraxia(HPO:0002186) MedDRA: |
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Database Frequency: | 22 / 7739 | |||||||||||||||
Resource: |
All diseases associated with this symptom:
3-methylglutaconic aciduria type 3 | (Orphanet:67047) |
ALZHEIMER DISEASE 3 | (OMIM:607822) |
Aceruloplasminemia | (Orphanet:48818) |
Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia | (Orphanet:313808) |
Autosomal recessive spastic paraplegia type 21 | (Orphanet:101001) |
Cerebroretinal vasculopathy | (Orphanet:3421) |
FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 1 | (OMIM:105550) |
Frontotemporal dementia with motor neuron disease | (Orphanet:275872) |
Gerstmann-Straussler-Scheinker syndrome | (Orphanet:356) |
HERNS syndrome | (Orphanet:63261) |
Hereditary vascular retinopathy | (Orphanet:71291) |
Intellectual disability-developmental delay-contractures syndrome | (Orphanet:3454) |
LEUKOENCEPHALOPATHY, PROGRESSIVE, WITH OVARIAN FAILURE | (OMIM:615889) |
Lafora disease | (Orphanet:501) |
MIGRAINE, FAMILIAL HEMIPLEGIC, 2 | (OMIM:602481) |
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2 | (OMIM:615157) |
Marden-Walker syndrome | (Orphanet:2461) |
Nasu-Hakola disease | (Orphanet:2770) |
Progressive non-fluent aphasia | (Orphanet:100070) |
RETT SYNDROME, CONGENITAL VARIANT | (OMIM:613454) |
Retinal vasculopathy and cerebral leukodystrophy | (Orphanet:247691) |
Spinocerebellar ataxia type 17 | (Orphanet:98759) |