Brisk reflexes
Symptom Information:
Symptom ID: | HPO:0001348 | ||
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 central motor function(HPO:0011442) Abnormal pyramidal signs(HPO:0007256) Hyperreflexia(HPO:0001347) Brisk reflexes(HPO:0001348) MedDRA: |
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Database Frequency: | 15 / 7739 | ||
Resource: |
All diseases associated with this symptom:
AMYOTROPHIC LATERAL SCLEROSIS 17 | (OMIM:614696) |
Adenylosuccinate lyase deficiency | (Orphanet:46) |
Autosomal dominant spastic paraplegia type 10 | (Orphanet:100991) |
Autosomal dominant spastic paraplegia type 12 | (Orphanet:100993) |
Autosomal dominant spastic paraplegia type 4 | (Orphanet:100985) |
Autosomal recessive spastic paraplegia type 15 | (Orphanet:100996) |
Autosomal recessive spastic paraplegia type 46 | (Orphanet:320391) |
Combined oxidative phosphorylation defect type 14 | (Orphanet:319519) |
DYSTONIA WITH CEREBELLAR ATROPHY | (OMIM:611694) |
Paraplegia - intellectual deficit - hyperkeratosis | (Orphanet:2824) |
Pontocerebellar hypoplasia type 6 | (Orphanet:166073) |
Pyruvate dehydrogenase E2 deficiency | (Orphanet:79244) |
Pyruvate dehydrogenase E3-binding protein deficiency | (Orphanet:255182) |
Spondyloepiphyseal dysplasia, Reardon type | (Orphanet:163662) |
X-linked immunoneurologic disorder | (Orphanet:2571) |