Brisk reflexes

Symptom Information:

Symptom ID: HPO:0001348
Synonyms:
Brisk reflexes [OMIM:Brisk reflexes]
Brisk reflexes (1 patient) [OMIM:Brisk reflexes (1 patient)]
Quality:
Cross references:
OMIM: "Brisk reflexes" [OMIM:Brisk reflexes]
OMIM: "Brisk reflexes (1 patient)" [OMIM:Brisk reflexes (1 patient)]
Is a (Direct Parents):
HPO         Hyperreflexia
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)
             Abnormality of central motor function(HPO:0011442)
                Abnormal pyramidal signs(HPO:0007256)
                   Hyperreflexia(HPO:0001347)
                      Brisk reflexes(HPO:0001348)
MedDRA:
Database Frequency: 15 / 7739
Resource:

All diseases associated with this symptom:

AMYOTROPHIC LATERAL SCLEROSIS 17 (OMIM:614696)
Adenylosuccinate lyase deficiency (Orphanet:46)
Autosomal dominant spastic paraplegia type 10 (Orphanet:100991)
Autosomal dominant spastic paraplegia type 12 (Orphanet:100993)
Autosomal dominant spastic paraplegia type 4 (Orphanet:100985)
Autosomal recessive spastic paraplegia type 15 (Orphanet:100996)
Autosomal recessive spastic paraplegia type 46 (Orphanet:320391)
Combined oxidative phosphorylation defect type 14 (Orphanet:319519)
DYSTONIA WITH CEREBELLAR ATROPHY (OMIM:611694)
Paraplegia - intellectual deficit - hyperkeratosis (Orphanet:2824)
Pontocerebellar hypoplasia type 6 (Orphanet:166073)
Pyruvate dehydrogenase E2 deficiency (Orphanet:79244)
Pyruvate dehydrogenase E3-binding protein deficiency (Orphanet:255182)
Spondyloepiphyseal dysplasia, Reardon type (Orphanet:163662)
X-linked immunoneurologic disorder (Orphanet:2571)