Positive Romberg sign
Symptom Information:
Symptom ID: | HPO:0002403 | ||
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 morphology(HPO:0012639) Abnormal peripheral nervous system morphology(HPO:0000759) Peripheral neuropathy(HPO:0009830) Sensory impairment(HPO:0003474) Impaired proprioception(HPO:0010831) Positive Romberg sign(HPO:0002403) MedDRA: |
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Database Frequency: | 11 / 7739 | ||
Resource: |
All diseases associated with this symptom:
ATAXIA, SENSORY, 1, AUTOSOMAL DOMINANT | (OMIM:608984) |
Autosomal recessive progressive external ophthalmoplegia | (Orphanet:254886) |
CEREBELLAR ATAXIA, NEUROPATHY, AND VESTIBULAR AREFLEXIA SYNDROME | (OMIM:614575) |
Friedreich ataxia 1 | (OMIM:229300) |
Hereditary motor and sensory neuropathy type 6 | (Orphanet:90120) |
OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMALRECESSIVE | (OMIM:258650) |
Perrault Syndrome 5 | (OMIM:616138) |
Posterior column ataxia - retinitis pigmentosa | (Orphanet:88628) |
Sensory ataxic neuropathy-dysarthria-ophthalmoparesis | (Orphanet:70595) |
Spinocerebellar ataxia type 17 | (Orphanet:98759) |
Spinocerebellar ataxia with epilepsy | (Orphanet:254881) |