Tongue fasciculations
Symptom Information:
Symptom ID: | HPO:0001308 | ||||||
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 movement(HPO:0100022) Muscle fibrillation(HPO:0010546) Tongue fasciculations(HPO:0001308) Involuntary movements(HPO:0004305) Fasciculations(HPO:0002380) Tongue fasciculations(HPO:0001308) Abnormality of the musculature(HPO:0003011) Abnormality of muscle physiology(HPO:0011804) Involuntary movements(HPO:0004305) Fasciculations(HPO:0002380) Tongue fasciculations(HPO:0001308) Abnormality of head or neck(HPO:0000152) Abnormality of the head(HPO:0000234) Abnormality of the face(HPO:0000271) Abnormality of the mouth(HPO:0000153) Abnormality of the oral cavity(HPO:0000163) Abnormality of the tongue(HPO:0000157) Tongue fasciculations(HPO:0001308) MedDRA: |
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Database Frequency: | 18 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
AMYOTROPHIC LATERAL SCLEROSIS 12 | (OMIM:613435) |
BROWN-VIALETTO-VAN LAERE SYNDROME 1 | (OMIM:211530) |
BROWN-VIALETTO-VAN LAERE SYNDROME 2 | (OMIM:614707) |
Charcot-Marie-Tooth disease type 4C | (Orphanet:99949) |
Combined oxidative phosphorylation defect type 11 | (Orphanet:324535) |
Hereditary myoclonus - progressive distal muscular atrophy | (Orphanet:2590) |
PONTOCEREBELLAR HYPOPLASIA, TYPE 1B | (OMIM:614678) |
Proximal spinal muscular atrophy | (Orphanet:70) |
Proximal spinal muscular atrophy type 1 | (Orphanet:83330) |
Proximal spinal muscular atrophy type 2 | (Orphanet:83418) |
Proximal spinal muscular atrophy type 3 | (Orphanet:83419) |
Proximal spinal muscular atrophy type 4 | (Orphanet:83420) |
Riboflavin transporter deficiency | (Orphanet:97229) |
Severe X-linked mitochondrial encephalomyopathy | (Orphanet:238329) |
Spinocerebellar ataxia type 36 | (Orphanet:276198) |
Spondyloepiphyseal dysplasia, Reardon type | (Orphanet:163662) |
Sudden infant death - dysgenesis of the testes | (Orphanet:168593) |
X-linked distal arthrogryposis multiplex congenita | (Orphanet:1145) |