Scanning speech
Symptom Information:
Symptom ID: | HPO:0002168 | ||
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) Scanning speech(HPO:0002168) MedDRA: |
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Database Frequency: | 10 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Aceruloplasminemia | (Orphanet:48818) |
Ataxia - hypogonadism - choroidal dystrophy | (Orphanet:1180) |
Autosomal recessive spastic ataxia of Charlevoix-Saguenay | (Orphanet:98) |
CLN9 disease | (Orphanet:228357) |
OLIVOPONTOCEREBELLAR ATROPHY II, AUTOSOMAL RECESSIVE | (OMIM:258300) |
PELIZAEUS-MERZBACHER DISEASE | (OMIM:312080) |
Spinocerebellar ataxia type 1 | (Orphanet:98755) |
Spinocerebellar ataxia type 10 | (Orphanet:98761) |
Spinocerebellar ataxia type 15/16 | (Orphanet:98769) |
Spinocerebellar ataxia type 21 | (Orphanet:98773) |