Aphasia

Symptom Information:

Symptom ID: HPO:0002381
Synonyms:
Aphasia (finding) [Orphanet:43480]
Dysphasia (finding) [Orphanet:43480]
Dysphasia [Orphanet:43480]
Aphasia [Orphanet:43480]
Aphasia [OMIM:Aphasia]
Speech troubles/aphasia/dysphasia/echolalia/mutism/logorrhea/dysprosodia [Orphanet:43480]
Aphasia [MedDRA:10002948]
Anomia [MedDRA:10002948]
Aphasia motor [MedDRA:10002948]
Aphasia nominal [MedDRA:10002948]
Aphasia sensory [MedDRA:10002948]
Broca's aphasia [MedDRA:10002948]
Dysphasia [MedDRA:10002948]
Expressive aphasia [MedDRA:10002948]
Expressive dysphasia [MedDRA:10002948]
Fluent aphasia [MedDRA:10002948]
Jargon aphasia [MedDRA:10002948]
Nominal aphasia [MedDRA:10002948]
Non-fluent aphasia [MedDRA:10002948]
Receptive aphasia [MedDRA:10002948]
Receptive dysphasia [MedDRA:10002948]
Speech loss [MedDRA:10002948]
Dysnomia [MedDRA:10002948]
Amnesic aphasia [MedDRA:10002948]
Amnestic aphasia [MedDRA:10002948]
Word finding difficulty [MedDRA:10002948]
Paraphasia [MedDRA:10002948]
Nominal dysphasia [MedDRA:10002948]
Dysnomia [OMIM:Dysnomia]
Expressive dysphasia [OMIM:Expressive dysphasia]
Word-finding difficulties [OMIM:Word-finding difficulties]
Dysprosody [MedDRA:10013977]
Dysprosody [Orphanet:43480]
Logorrhoea [MedDRA:10024796]
Logorrhea [Orphanet:43480]
Logorrhea (finding) [Orphanet:43480]
Volubility (finding) [Orphanet:43480]
Volubility [Orphanet:43480]
Quality:
Cross references:
HPO:0002357 "Dysphasia" [Orphanet:43480]
Orphanet:43480 "Speech troubles/aphasia/dysphasia/echolalia/mutism/logorrhea/dysprosodia" [Orphanet:43480]
OMIM: "Aphasia" [OMIM:Aphasia]
OMIM: "Dysnomia" [OMIM:Dysnomia]
OMIM: "Expressive dysphasia" [OMIM:Expressive dysphasia]
OMIM: "Word-finding difficulties" [OMIM:Word-finding difficulties]
UMLS:C0003537 "Aphasia" [HPO:0002381]
UMLS:C0973461 "Dysphasia" [Orphanet:43480]
UMLS:C0003537 "Aphasia" [Orphanet:43480]
UMLS:C0854737 "Dysprosody" [Orphanet:43480]
UMLS:C0233719 "Volubility" [Orphanet:43480]
Is a (Direct Parents):
HPO         Neurological speech impairment
Orphanet Functional anomalies of the nervous system
Orphanet Mutism
MedDRA Specific cognitive ability disturbances
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)
                Neurological speech impairment(HPO:0002167)
                   Aphasia(HPO:0002381)
MedDRA:
Database Frequency: 27 / 7739
Resource:

All diseases associated with this symptom:

3-methylglutaconic aciduria type 3 (Orphanet:67047)
48,XXYY syndrome (Orphanet:10)
Aceruloplasminemia (Orphanet:48818)
Argininemia (Orphanet:90)
Bardet-Biedl syndrome (Orphanet:110)
CADASIL (Orphanet:136)
Cerebroretinal vasculopathy (Orphanet:3421)
Creutzfeldt-Jakob disease (Orphanet:204)
Cystinosis (Orphanet:213)
FRONTOTEMPORAL DEMENTIA (OMIM:600274)
Flynn-Aird syndrome (Orphanet:2047)
Glycogen storage disease due to acid maltase deficiency (Orphanet:365)
INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUTFRONTOTEMPORAL DEMENTIA 1 (OMIM:167320)
Inherited Creutzfeldt-Jakob disease (Orphanet:282166)
Intellectual deficit, X-linked, Wilson type (Orphanet:85290)
L1 syndrome (Orphanet:275543)
MASA syndrome (Orphanet:2466)
MELAS (Orphanet:550)
MIGRAINE, FAMILIAL HEMIPLEGIC, 2 (OMIM:602481)
Niemann-Pick disease type C (Orphanet:646)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Progressive non-fluent aphasia (Orphanet:100070)
Rolandic epilepsy - speech dyspraxia (Orphanet:163721)
Sneddon syndrome (Orphanet:820)
Tyrosinemia type 2 (Orphanet:28378)
Wilson-Turner syndrome (Orphanet:3459)
X-linked complicated spastic paraplegia type 1 (Orphanet:306617)