Knee clonus
Symptom Information:
| Symptom ID: | HPO:0011449 | ||
| Synonyms: |
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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) Clonus(HPO:0002169) Knee clonus(HPO:0011449) MedDRA: |
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| Database Frequency: | 10 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| Autosomal dominant spastic paraplegia type 10 | (Orphanet:100991) |
| Autosomal dominant spastic paraplegia type 12 | (Orphanet:100993) |
| Autosomal dominant spastic paraplegia type 19 | (Orphanet:100999) |
| Autosomal dominant spastic paraplegia type 6 | (Orphanet:100988) |
| Autosomal recessive spastic paraplegia type 11 | (Orphanet:2822) |
| Autosomal recessive spastic paraplegia type 20 | (Orphanet:101000) |
| Autosomal recessive spastic paraplegia type 46 | (Orphanet:320391) |
| Autosomal recessive spastic paraplegia type 55 | (Orphanet:320375) |
| Riboflavin transporter deficiency | (Orphanet:97229) |
| SPASTIC PARAPLEGIA, ATAXIA, AND MENTAL RETARDATION | (OMIM:607565) |