Echolalia

Symptom Information:

Symptom ID: HPO:0010529
Synonyms:
Echolalia (finding) [Orphanet:43480]
Echolalia [Orphanet:43480]
Echolalia [OMIM:Echolalia]
Speech troubles/aphasia/dysphasia/echolalia/mutism/logorrhea/dysprosodia [Orphanet:43480]
Echolalia [MedDRA:10014127]
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:
Orphanet:43480 "Speech troubles/aphasia/dysphasia/echolalia/mutism/logorrhea/dysprosodia" [Orphanet:43480]
OMIM: "Echolalia" [OMIM:Echolalia]
UMLS:C0013528 "Echolalia" [HPO:0010529]
UMLS:C0013528 "Echolalia" [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
HPO         Abnormal emotion/affect behavior
MedDRA Stereotypies and automatisms
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:
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)