Bulbar palsy
Symptom Information:
Symptom ID: | HPO:0001283 | ||||||||
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 musculature(HPO:0003011) Abnormality of muscle physiology(HPO:0011804) Muscle weakness(HPO:0001324) Bulbar palsy(HPO:0001283) MedDRA: Nervous system disorders(MedDRA:10029205) Cranial nerve disorders (excl neoplasms)(MedDRA:10011305) Mixed cranial nerve disorders(MedDRA:10027755) Bulbar palsy(HPO:0001283) |
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Database Frequency: | 31 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
Adrenomyeloneuropathy | (Orphanet:139399) |
Amyotrophic lateral sclerosis-parkinsonism-dementia complex | (Orphanet:90020) |
Autosomal dominant spastic paraplegia type 31 | (Orphanet:101011) |
BROWN-VIALETTO-VAN LAERE SYNDROME 1 | (OMIM:211530) |
BROWN-VIALETTO-VAN LAERE SYNDROME 2 | (OMIM:614707) |
Congenital fiber-type disproportion myopathy | (Orphanet:2020) |
Congenital myopathy with excess of thin filaments | (Orphanet:98904) |
Desminopathy | (Orphanet:98909) |
Distal myopathy with vocal cord weakness | (Orphanet:600) |
FAZIO-LONDE DISEASE | (OMIM:211500) |
FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 2 | (OMIM:615911) |
Familial amyloidosis, Finnish type | (Orphanet:85448) |
Gaucher disease type 2 | (Orphanet:77260) |
Gaucher disease type 3 | (Orphanet:77261) |
Glycogen storage disease due to acid maltase deficiency, late-onset | (Orphanet:420429) |
Kennedy disease | (Orphanet:481) |
METACHROMATIC LEUKODYSTROPHY | (OMIM:250100) |
MYASTHENIC SYNDROME, CONGENITAL, 10 | (OMIM:254300) |
MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL | (OMIM:608930) |
MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL | (OMIM:605809) |
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION | (OMIM:255310) |
NEMALINE MYOPATHY 10 | (OMIM:616165) |
NEMALINE MYOPATHY 2 | (OMIM:256030) |
Nemaline myopathy | (Orphanet:607) |
Postsynaptic congenital myasthenic syndromes | (Orphanet:98913) |
Presynaptic congenital myasthenic syndromes | (Orphanet:98914) |
Riboflavin transporter deficiency | (Orphanet:97229) |
Spinocerebellar ataxia type 1 | (Orphanet:98755) |
Spondyloepiphyseal dysplasia, Reardon type | (Orphanet:163662) |
Steinert myotonic dystrophy | (Orphanet:273) |
X-linked cerebral adrenoleukodystrophy | (Orphanet:139396) |