Apraxia

Symptom Information:

Symptom ID: HPO:0002186
Synonyms:
Apraxias [HPO:0002186]
Apraxia (finding) [Orphanet:43320]
Apraxias [Orphanet:43320]
Apraxia [OMIM:Apraxia]
Execution movement disorder/dysmetria/bradykinesia/akinesia/apraxia [Orphanet:43320]
Apraxia [Orphanet:43320]
Apraxia [MedDRA:10003062]
Constructional apraxia [MedDRA:10003062]
Dressing apraxia [MedDRA:10003062]
Gaze apraxia [MedDRA:10003062]
Ideational apraxia [MedDRA:10003062]
Ideomotor apraxia [MedDRA:10003062]
Apraxia of eyelid [MedDRA:10003062]
Constructional apraxia (in a subset of patients) [OMIM:Constructional apraxia (in a subset of patients)]
Execution movement disorder [Orphanet:43320]
Quality:
Cross references:
Orphanet:43320 "Execution movement disorder/dysmetria/bradykinesia/akinesia/apraxia" [Orphanet:43320]
OMIM: "Apraxia" [OMIM:Apraxia]
OMIM: "Constructional apraxia (in a subset of patients)" [OMIM:Constructional apraxia (in a subset of patients)]
UMLS:C0003635 "Apraxia" [HPO:0002186]
UMLS:C0003635 "Apraxias" [Orphanet:43320]
Is a (Direct Parents):
HPO         Limb apraxia
Orphanet Dysmetria
HPO         Abnormality of higher mental function
Orphanet [DEL]Motor deficit/trouble
MedDRA Specific cognitive ability disturbances
HPO         Abnormality of central motor function
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:
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)