Hyperactive deep tendon reflexes

Symptom Information:

Symptom ID: HPO:0006801
Synonyms:
Brisk deep tendon reflexes [HPO:0006801]
Brisk deep tendon reflexes [OMIM:Brisk deep tendon reflexes]
Hyperactive deep tendon reflexes [OMIM:Hyperactive deep tendon reflexes]
Quality:
Cross references:
OMIM: "Brisk deep tendon reflexes" [OMIM:Brisk deep tendon reflexes]
OMIM: "Hyperactive deep tendon reflexes" [OMIM:Hyperactive deep tendon reflexes]
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)
                      Hyperactive deep tendon reflexes(HPO:0006801)
MedDRA:
Database Frequency: 21 / 7739
Resource:

All diseases associated with this symptom:

Ataxia - pancytopenia (Orphanet:2585)
Autosomal recessive nonsyndromic intellectual deficit (Orphanet:88616)
Autosomal recessive spastic paraplegia type 11 (Orphanet:2822)
Autosomal recessive spastic paraplegia type 45 (Orphanet:320396)
CHOROID PLEXUS CALCIFICATION AND MENTAL RETARDATION (OMIM:215480)
CHROMOSOME 17p13.1 DELETION SYNDROME (OMIM:613776)
Dyschromatosis symmetrica hereditaria (Orphanet:41)
Hurler-Scheie syndrome (Orphanet:93476)
Hyperlysinemia, type I (OMIM:238700)
Hyperornithinemia-hyperammonemia-homocitrullinuria (Orphanet:415)
Krabbe disease (Orphanet:487)
Leigh syndrome (Orphanet:506)
Microcephaly-capillary malformation syndrome (Orphanet:294016)
OCULODENTODIGITAL DYSPLASIA (OMIM:164200)
Oculodentodigital dysplasia (Orphanet:2710)
Pontocerebellar hypoplasia, type 9 (OMIM:615809)
Pyruvate dehydrogenase E2 deficiency (Orphanet:79244)
Simpson-Golabi-Behmel syndrome type 2 (Orphanet:79022)
Spastic paraplegia 63, autosomal recessive (OMIM:615686)
Spastic paraplegia 64, autosomal recessive (OMIM:615683)
X-linked Charcot-Marie-Tooth disease type 5 (Orphanet:99014)