Areflexia of lower limbs

Symptom Information:

Symptom ID: HPO:0002522
Synonyms:
Absent lower limb tendon reflexes [HPO:0002522]
Areflexia in lower limbs [HPO:0002522]
Areflexia of the lower limbs [HPO:0002522]
Areflexia, lower limbs [HPO:0002522]
Absent lower limb tendon reflexes [OMIM:Absent lower limb tendon reflexes]
Areflexia in lower limbs [OMIM:Areflexia in lower limbs]
Areflexia of lower limbs [OMIM:Areflexia of lower limbs]
Areflexia of the lower limbs [OMIM:Areflexia of the lower limbs]
Areflexia, lower limbs [OMIM:Areflexia, lower limbs]
Quality:
Cross references:
OMIM: "Absent lower limb tendon reflexes" [OMIM:Absent lower limb tendon reflexes]
OMIM: "Areflexia in lower limbs" [OMIM:Areflexia in lower limbs]
OMIM: "Areflexia of lower limbs" [OMIM:Areflexia of lower limbs]
OMIM: "Areflexia of the lower limbs" [OMIM:Areflexia of the lower limbs]
OMIM: "Areflexia, lower limbs" [OMIM:Areflexia, lower limbs]
Is a (Direct Parents):
HPO         Areflexia
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:
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)