Ankle clonus

Symptom Information:

Symptom ID: HPO:0011448
Synonyms:
Ankle clonus [OMIM:Ankle clonus]
Ankle clonus (in some) [OMIM:Ankle clonus (in some)]
Quality:
Cross references:
OMIM: "Ankle clonus" [OMIM:Ankle clonus]
OMIM: "Ankle clonus (in some)" [OMIM:Ankle clonus (in some)]
Is a (Direct Parents):
HPO         Clonus
HPO         Abnormality of the ankles
HPO         Abnormality of the knee
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)
                   Abnormality of the lower limb(HPO:0002814)
                      Abnormality of lower limb joint(HPO:0100491)
                         Abnormality of the ankles(HPO:0003028)
                            Ankle clonus(HPO:0011448)
                         Abnormality of the knee(HPO:0002815)
                            Ankle clonus(HPO:0011448)
             Abnormal joint morphology(HPO:0001367)
                Abnormality of lower limb joint(HPO:0100491)
                   Abnormality of the ankles(HPO:0003028)
                      Ankle clonus(HPO:0011448)
                   Abnormality of the knee(HPO:0002815)
                      Ankle clonus(HPO:0011448)
       Abnormality of the nervous system(HPO:0000707)
          Abnormality of nervous system physiology(HPO:0012638)
             Abnormality of movement(HPO:0100022)
                Clonus(HPO:0002169)
                   Ankle clonus(HPO:0011448)
MedDRA:
Database Frequency: 31 / 7739
Resource:

All diseases associated with this symptom:

ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTICATROPHY AND MENTAL RETARDATION (OMIM:270500)
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 31 (Orphanet:101011)
Autosomal dominant spastic paraplegia type 37 (Orphanet:171612)
Autosomal dominant spastic paraplegia type 4 (Orphanet:100985)
Autosomal dominant spastic paraplegia type 6 (Orphanet:100988)
Autosomal recessive spastic paraplegia type 11 (Orphanet:2822)
Autosomal recessive spastic paraplegia type 15 (Orphanet:100996)
Autosomal recessive spastic paraplegia type 20 (Orphanet:101000)
Autosomal recessive spastic paraplegia type 30 (Orphanet:101010)
Autosomal recessive spastic paraplegia type 32 (Orphanet:171622)
Autosomal recessive spastic paraplegia type 35 (Orphanet:171629)
Autosomal recessive spastic paraplegia type 45 (Orphanet:320396)
Autosomal recessive spastic paraplegia type 46 (Orphanet:320391)
BROWN-VIALETTO-VAN LAERE SYNDROME 1 (OMIM:211530)
Bilateral frontoparietal polymicrogyria (Orphanet:101070)
CAMOS syndrome (Orphanet:83472)
CHROMOSOME 17p13.1 DELETION SYNDROME (OMIM:613776)
Classical phenylketonuria (Orphanet:79254)
HYPERREFLEXIA (OMIM:145290)
Hyperornithinemia-hyperammonemia-homocitrullinuria (Orphanet:415)
Leber plus disease (Orphanet:99718)
Pontine tegmental cap dysplasia (Orphanet:269229)
Riboflavin transporter deficiency (Orphanet:97229)
SPASTIC PARAPLEGIA, ATAXIA, AND MENTAL RETARDATION (OMIM:607565)
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 16 (OMIM:615768)
Spastic paraplegia 33, autosomal dominant (OMIM:610244)
Spondyloepiphyseal dysplasia, Reardon type (Orphanet:163662)
WARBURG MICRO SYNDROME 3 (OMIM:614222)