Mutism

Symptom Information:

Symptom ID: HPO:0002300
Synonyms:
Mutism (finding) [Orphanet:43480]
Unable to talk (finding) [Orphanet:43480]
Unable to talk [Orphanet:43480]
Mutism [Orphanet:43480]
Mutism [OMIM:Mutism]
Speech troubles/aphasia/dysphasia/echolalia/mutism/logorrhea/dysprosodia [Orphanet:43480]
Mutism [MedDRA:10028403]
Mutism NEC [MedDRA:10028403]
Silence [MedDRA:10028403]
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: "Mutism" [OMIM:Mutism]
UMLS:C0026884 "Mutism" [HPO:0002300]
UMLS:C0278249 "Unable to talk" [Orphanet:43480]
UMLS:C0026884 "Mutism" [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
HPO         Abnormal emotion/affect behavior
MedDRA Speech and language abnormalities
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)
                   Mutism(HPO:0002300)
                Behavioral abnormality(HPO:0000708)
                   Abnormal emotion/affect behavior(HPO:0100851)
                      Mutism(HPO:0002300)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Neurological disorders NEC(MedDRA:10029305)
       Speech and language abnormalities(MedDRA:10041460)
          Mutism(HPO:0002300)
Database Frequency: 28 / 7739
Resource:

All diseases associated with this symptom:

3-methylglutaconic aciduria type 3 (Orphanet:67047)
48,XXYY syndrome (Orphanet:10)
Aceruloplasminemia (Orphanet:48818)
Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (Orphanet:313808)
Argininemia (Orphanet:90)
Bardet-Biedl syndrome (Orphanet:110)
Behavioral variant of frontotemporal dementia (Orphanet:275864)
Biotin-responsive basal ganglia disease (Orphanet:65284)
CADASIL (Orphanet:136)
CLN9 disease (Orphanet:228357)
Cerebroretinal vasculopathy (Orphanet:3421)
Christianson syndrome (Orphanet:85278)
Classical progressive supranuclear palsy (Orphanet:240071)
Cystinosis (Orphanet:213)
Glycogen storage disease due to acid maltase deficiency (Orphanet:365)
Huntington disease-like 3 (Orphanet:157946)
MELAS (Orphanet:550)
Multiple acyl-CoA dehydrogenase deficiency (Orphanet:26791)
Neuroferritinopathy (Orphanet:157846)
Niemann-Pick disease type C (Orphanet:646)
Progressive non-fluent aphasia (Orphanet:100070)
Rapid-onset dystonia-parkinsonism (Orphanet:71517)
Richards-Rundle syndrome (Orphanet:1399)
SUPRANUCLEAR PALSY, PROGRESSIVE, 1 (OMIM:601104)
Spinocerebellar ataxia type 17 (Orphanet:98759)
Thiamine-responsive encephalopathy (Orphanet:199348)
Tyrosinemia type 2 (Orphanet:28378)
Wilson-Turner syndrome (Orphanet:3459)