Generalized hyperreflexia

Symptom Information:

Symptom ID: HPO:0007034
Synonyms:
Hyperreflexia [Orphanet:43360]
Hyperreflexia (finding) [Orphanet:43360]
Generalized hyperreflexia [OMIM:Generalized hyperreflexia]
Hypereflexia [Orphanet:43360]
Hyperreflexia [MedDRA:10020745]
Achilles tendon reflex exaggerated [MedDRA:10020745]
Exaggerated reflexes [MedDRA:10020745]
Increased reflexes [MedDRA:10020745]
Patellar tendon reflex increased [MedDRA:10020745]
Reflex positive pathological [MedDRA:10020745]
Reflexes increased [MedDRA:10020745]
Reflexes tendon increased [MedDRA:10020745]
Tendon reflex exaggerated [MedDRA:10020745]
Hyperreflexia (1 patient) [OMIM:Hyperreflexia (1 patient)]
Hyperreflexia (33%) [OMIM:Hyperreflexia (33%)]
Hyperreflexia (70%) [OMIM:Hyperreflexia (70%)]
Hyperreflexia (early) [OMIM:Hyperreflexia (early)]
Hyperreflexia (in 2 of 7 patients) [OMIM:Hyperreflexia (in 2 of 7 patients)]
Hyperreflexia (in some patients) [OMIM:Hyperreflexia (in some patients)]
Hyperreflexia (in some) [OMIM:Hyperreflexia (in some)]
Hyperreflexia (later) [OMIM:Hyperreflexia (later)]
Hyperreflexia (less common) [OMIM:Hyperreflexia (less common)]
Hyperreflexia (particularly in lower extremities, more prevalent in adolescents and adults) [OMIM:Hyperreflexia (particularly in lower extremities, more prevalent in adolescents and adults)]
Hyperreflexia (some patients) [OMIM:Hyperreflexia (some patients)]
Hyperreflexia (type I) [OMIM:Hyperreflexia (type I)]
Hyperreflexia (uncommon) [OMIM:Hyperreflexia (uncommon)]
Increased tendon reflex [OMIM:Increased tendon reflex]
Quality:
Cross references:
HPO:0002267 "Exaggerated startle response" [Orphanet:43360]
HPO:0001347 "Hyperreflexia" [Orphanet:43360]
Orphanet:43360 "Hypereflexia" [Orphanet:43360]
OMIM: "Generalized hyperreflexia" [OMIM:Generalized hyperreflexia]
OMIM: "Hyperreflexia (1 patient)" [OMIM:Hyperreflexia (1 patient)]
OMIM: "Hyperreflexia (33%)" [OMIM:Hyperreflexia (33%)]
OMIM: "Hyperreflexia (70%)" [OMIM:Hyperreflexia (70%)]
OMIM: "Hyperreflexia (early)" [OMIM:Hyperreflexia (early)]
OMIM: "Hyperreflexia (in 2 of 7 patients)" [OMIM:Hyperreflexia (in 2 of 7 patients)]
OMIM: "Hyperreflexia (in some patients)" [OMIM:Hyperreflexia (in some patients)]
OMIM: "Hyperreflexia (in some)" [OMIM:Hyperreflexia (in some)]
OMIM: "Hyperreflexia (later)" [OMIM:Hyperreflexia (later)]
OMIM: "Hyperreflexia (less common)" [OMIM:Hyperreflexia (less common)]
OMIM: "Hyperreflexia (particularly in lower extremities, more prevalent in adolescents and adults)" [OMIM:Hyperreflexia (particularly in lower extremities, more prevalent in adolescents and adults)]
OMIM: "Hyperreflexia (some patients)" [OMIM:Hyperreflexia (some patients)]
OMIM: "Hyperreflexia (type I)" [OMIM:Hyperreflexia (type I)]
OMIM: "Hyperreflexia (uncommon)" [OMIM:Hyperreflexia (uncommon)]
OMIM: "Increased tendon reflex" [OMIM:Increased tendon reflex]
UMLS:C0151889 "Hyperreflexia" [Orphanet:43360]
Is a (Direct Parents):
HPO         Hyperreflexia
Orphanet [DEL]Motor deficit/trouble
MedDRA Abnormal reflexes
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)
                      Generalized hyperreflexia(HPO:0007034)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Neurological disorders NEC(MedDRA:10029305)
       Abnormal reflexes(MedDRA:10000171)
          Generalized hyperreflexia(HPO:0007034)
Database Frequency: 33 / 7739
Resource:

All diseases associated with this symptom:

3-methylglutaconic aciduria type 1 (Orphanet:67046)
3-methylglutaconic aciduria type 3 (Orphanet:67047)
6-pyruvoyl-tetrahydropterin synthase deficiency (Orphanet:13)
Autosomal dominant Charcot-Marie-Tooth disease type 2A2 (Orphanet:99947)
Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures (Orphanet:363454)
Autosomal dominant dopa-responsive dystonia (Orphanet:98808)
Autosomal recessive spastic paraplegia type 43 (Orphanet:320370)
CARASIL (Orphanet:199354)
Classical phenylketonuria (Orphanet:79254)
Congenital myopathy with excess of thin filaments (Orphanet:98904)
FAZIO-LONDE DISEASE (OMIM:211500)
Gaucher disease type 2 (Orphanet:77260)
Huntington disease (Orphanet:399)
Hyperornithinemia-hyperammonemia-homocitrullinuria (Orphanet:415)
Lethal ataxia with deafness and optic atrophy (Orphanet:1187)
METACHROMATIC LEUKODYSTROPHY (OMIM:250100)
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2 (OMIM:615157)
Maternal hyperphenylalaninemia (Orphanet:2209)
Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus (Orphanet:83473)
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency (Orphanet:1194)
Multiple congenital anomalies - hypotonia - seizures syndrome (Orphanet:280633)
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A (OMIM:256600)
NEUROPATHY, HEREDITARY SENSORY, TYPE ID (OMIM:613708)
Neurodegeneration with brain iron accumulation due to C19orf12 mutation (Orphanet:289560)
PARKINSON DISEASE 6, AUTOSOMAL RECESSIVE EARLY-ONSET (OMIM:605909)
Pontine tegmental cap dysplasia (Orphanet:269229)
Sialidosis type 1 (Orphanet:812)
Spectrin-associated autosomal recessive cerebellar ataxia (Orphanet:352403)
Spinocerebellar ataxia type 1 (Orphanet:98755)
Spinocerebellar ataxia type 19/22 (Orphanet:98772)
Sporadic Leigh syndrome (Orphanet:255199)
Williams syndrome (Orphanet:904)
X-linked parkinsonism-spasticity syndrome (Orphanet:363654)