Echolalia
Symptom Information:
Symptom ID: | HPO:0010529 | ||||||||||||
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) Behavioral abnormality(HPO:0000708) Abnormal emotion/affect behavior(HPO:0100851) Echolalia(HPO:0010529) Neurological speech impairment(HPO:0002167) Echolalia(HPO:0010529) MedDRA: |
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Database Frequency: | 20 / 7739 | ||||||||||||
Resource: |
All diseases associated with this symptom:
17p11.2 microduplication syndrome | (Orphanet:1713) |
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) |
Cystinosis | (Orphanet:213) |
Frontotemporal dementia | (Orphanet:282) |
GILLES DE LA TOURETTE SYNDROME | (OMIM:137580) |
Glycogen storage disease due to acid maltase deficiency | (Orphanet:365) |
Intellectual deficit, X-linked, Nascimento type | (Orphanet:163956) |
MELAS | (Orphanet:550) |
Monosomy 5p | (Orphanet:281) |
Niemann-Pick disease type C | (Orphanet:646) |
PICK DISEASE OF BRAIN | (OMIM:172700) |
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency | (Orphanet:88618) |
Tyrosinemia type 2 | (Orphanet:28378) |
Wilson-Turner syndrome | (Orphanet:3459) |