Speech apraxia
Symptom Information:
Symptom ID: | HPO:0011098 | |||
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) Apraxia(HPO:0002186) Speech apraxia(HPO:0011098) Abnormality of central motor function(HPO:0011442) Apraxia(HPO:0002186) Speech apraxia(HPO:0011098) MedDRA: |
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Database Frequency: | 9 / 7739 | |||
Resource: |
All diseases associated with this symptom:
Epileptic encephalopathy with continuous spike-and-wave during sleep | (Orphanet:725) |
Hyperornithinemia-hyperammonemia-homocitrullinuria | (Orphanet:415) |
Landau-Kleffner syndrome | (Orphanet:98818) |
MELAS | (Orphanet:550) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 17 | (OMIM:615009) |
Moyamoya disease - short stature - facial dysmorphism - hypergonadotropic hypogonadism | (Orphanet:280679) |
NARP syndrome | (Orphanet:644) |
ROLANDIC EPILEPSY, MENTAL RETARDATION, AND SPEECH DYSPRAXIA, X-LINKED | (OMIM:300643) |
Rolandic epilepsy - speech dyspraxia | (Orphanet:163721) |