Bulbar palsy

Symptom Information:

Symptom ID: HPO:0001283
Synonyms:
Bulbar muscle weakness [HPO:0001283]
Bulbar palsies [HPO:0001283]
Bulbar weakness [HPO:0001283]
Bulbar muscle weakness [OMIM:Bulbar muscle weakness]
Bulbar palsies [OMIM:Bulbar palsies]
Bulbar palsy [OMIM:Bulbar palsy]
Bulbar weakness [OMIM:Bulbar weakness]
Bulbar palsy [MedDRA:10006542]
Quality:
Cross references:
OMIM: "Bulbar muscle weakness" [OMIM:Bulbar muscle weakness]
OMIM: "Bulbar palsies" [OMIM:Bulbar palsies]
OMIM: "Bulbar palsy" [OMIM:Bulbar palsy]
OMIM: "Bulbar weakness" [OMIM:Bulbar weakness]
Is a (Direct Parents):
HPO         Muscle weakness
MedDRA Mixed cranial nerve disorders
HPO         Abnormality of brainstem morphology
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)
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)