Mutism
Symptom Information:
Symptom ID: | HPO:0002300 | ||||||||||||||||
Synonyms: |
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Quality: | |||||||||||||||||
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) 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) |
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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) |