Generalized hyperreflexia
Symptom Information:
Symptom ID: | HPO:0007034 | |||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |