Areflexia of lower limbs
Symptom Information:
Symptom ID: | HPO:0002522 | |||||||||
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) Reduced tendon reflexes(HPO:0001315) Areflexia(HPO:0001284) Areflexia of lower limbs(HPO:0002522) MedDRA: |
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Database Frequency: | 16 / 7739 | |||||||||
Resource: |
All diseases associated with this symptom:
Autosomal dominant optic atrophy plus syndrome | (Orphanet:1215) |
Autosomal recessive limb-girdle muscular dystrophy type 2G | (Orphanet:34514) |
Distal hereditary motor neuropathy type 2 | (Orphanet:139525) |
Friedreich ataxia | (Orphanet:95) |
Friedreich ataxia 1 | (OMIM:229300) |
Giant axonal neuropathy | (Orphanet:643) |
MYOPATHY, TUBULAR AGGREGATE, 2 | (OMIM:615883) |
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIA | (OMIM:158590) |
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIB | (OMIM:608634) |
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC | (OMIM:613376) |
NEUROPATHY, CONGENITAL, WITH ARTHROGRYPOSIS MULTIPLEX | (OMIM:162370) |
Proximal spinal muscular atrophy type 3 | (Orphanet:83419) |
Proximal spinal muscular atrophy type 4 | (Orphanet:83420) |
Spinocerebellar ataxia type 25 | (Orphanet:101111) |
Tubular aggregate myopathy | (Orphanet:2593) |
X-linked Charcot-Marie-Tooth disease type 5 | (Orphanet:99014) |