Aphasia
Symptom Information:
Symptom ID: | HPO:0002381 | ||||||||||||||||||||||||||||||||||||||
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) Neurological speech impairment(HPO:0002167) Aphasia(HPO:0002381) MedDRA: |
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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) |