Lower limb hypertonia
Symptom Information:
Symptom ID: | HPO:0006895 | ||||
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 skeletal system(HPO:0000924) Abnormality of skeletal morphology(HPO:0011842) Abnormal appendicular skeleton morphology(HPO:0011844) Abnormality of limb bone morphology(HPO:0002813) Limb hypertonia(HPO:0002509) Lower limb hypertonia(HPO:0006895) Abnormality of the lower limb(HPO:0002814) Lower limb hypertonia(HPO:0006895) 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) Hypertonia(HPO:0001276) Limb hypertonia(HPO:0002509) Lower limb hypertonia(HPO:0006895) MedDRA: |
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Database Frequency: | 4 / 7739 | ||||
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All diseases associated with this symptom:
Autosomal recessive spastic paraplegia type 14 | (Orphanet:100995) |
PELGER-HUET ANOMALY | (OMIM:169400) |
Syndromic X-linked intellectual deficit due to JARID1C mutation | (Orphanet:85279) |
X-linked intellectual deficit - hypotonic face | (Orphanet:73220) |