Hyporeflexia of lower limbs

Symptom Information:

Symptom ID: HPO:0002600
Synonyms:
Hyporeflexia in lower limbs [HPO:0002600]
Hyporeflexia of the lower limbs [HPO:0002600]
Hyporeflexia, lower limbs [HPO:0002600]
Hyporeflexia/areflexia in lower limbs [HPO:0002600]
Hyporeflexia in lower limbs [OMIM:Hyporeflexia in lower limbs]
Hyporeflexia of lower limbs [OMIM:Hyporeflexia of lower limbs]
Hyporeflexia of the lower limbs [OMIM:Hyporeflexia of the lower limbs]
Hyporeflexia, lower limbs [OMIM:Hyporeflexia, lower limbs]
Hyporeflexia/areflexia in lower limbs [OMIM:Hyporeflexia/areflexia in lower limbs]
Quality:
Cross references:
OMIM: "Hyporeflexia in lower limbs" [OMIM:Hyporeflexia in lower limbs]
OMIM: "Hyporeflexia of lower limbs" [OMIM:Hyporeflexia of lower limbs]
OMIM: "Hyporeflexia of the lower limbs" [OMIM:Hyporeflexia of the lower limbs]
OMIM: "Hyporeflexia, lower limbs" [OMIM:Hyporeflexia, lower limbs]
OMIM: "Hyporeflexia/areflexia in lower limbs" [OMIM:Hyporeflexia/areflexia in lower limbs]
Is a (Direct Parents):
HPO         Hyporeflexia
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)
                Hyporeflexia(HPO:0001265)
                   Hyporeflexia of lower limbs(HPO:0002600)
MedDRA:
Database Frequency: 13 / 7739
Resource:

All diseases associated with this symptom:

Desminopathy (Orphanet:98909)
Distal hereditary motor neuropathy type 2 (Orphanet:139525)
Giant axonal neuropathy (Orphanet:643)
McLeod neuroacanthocytosis syndrome (Orphanet:59306)
Myotilin-related myofibrillar myopathy without spheroid body (Orphanet:98911)
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)
NEUROPATHY, HEREDITARY SENSORY, TYPE IF (OMIM:615632)
Pontocerebellar hypoplasia, type 9 (OMIM:615809)
Tubular aggregate myopathy (Orphanet:2593)
ZASP-related myofibrillar myopathy (Orphanet:98912)