Clonus
Symptom Information:
Symptom ID: | HPO:0002169 | ||||||||||||||||||||||
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 movement(HPO:0100022) Clonus(HPO:0002169) MedDRA: Nervous system disorders(MedDRA:10029205) Neurological disorders NEC(MedDRA:10029305) Neurological signs and symptoms NEC(MedDRA:10029306) Clonus(HPO:0002169) |
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Database Frequency: | 37 / 7739 | ||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Allan-Herndon-Dudley syndrome | (Orphanet:59) |
Amyotrophic lateral sclerosis type 4 | (Orphanet:357043) |
Argininemia | (Orphanet:90) |
Atypical Gaucher disease due to saposin C deficiency | (Orphanet:309252) |
Autosomal dominant spastic paraplegia type 29 | (Orphanet:101009) |
Autosomal dominant spastic paraplegia type 6 | (Orphanet:100988) |
Autosomal recessive ataxia due to ubiquinone deficiency | (Orphanet:139485) |
Autosomal recessive dopa-responsive dystonia | (Orphanet:101150) |
Autosomal recessive spastic paraplegia type 15 | (Orphanet:100996) |
Autosomal recessive spastic paraplegia type 24 | (Orphanet:101004) |
Autosomal recessive spastic paraplegia type 45 | (Orphanet:320396) |
Autosomal recessive spastic paraplegia type 53 | (Orphanet:319199) |
Autosomal recessive spastic paraplegia type 55 | (Orphanet:320375) |
CAMOS syndrome | (Orphanet:83472) |
Combined oxidative phosphorylation defect type 11 | (Orphanet:324535) |
Dihydropteridine reductase deficiency | (Orphanet:226) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 14 | (OMIM:614959) |
Gaucher disease type 3 | (Orphanet:77261) |
Hereditary sensory and autonomic neuropathy with spastic paraplegia | (Orphanet:139578) |
Hyperornithinemia-hyperammonemia-homocitrullinuria | (Orphanet:415) |
MELAS | (Orphanet:550) |
MERRF | (Orphanet:551) |
MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY | (OMIM:613668) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
PARTIAL LIPODYSTROPHY, CONGENITAL CATARACTS, AND NEURODEGENERATIONSYNDROME | (OMIM:606721) |
PONTOCEREBELLAR HYPOPLASIA, TYPE 2B | (OMIM:612389) |
PONTOCEREBELLAR HYPOPLASIA, TYPE 2D | (OMIM:613811) |
Pontocerebellar hypoplasia, type 9 | (OMIM:615809) |
Primary dystonia, DYT6 type | (Orphanet:98806) |
Pyruvate carboxylase deficiency | (Orphanet:3008) |
RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME, LETHAL NEONATAL | (OMIM:614498) |
Sensory ataxic neuropathy-dysarthria-ophthalmoparesis | (Orphanet:70595) |
Sialidosis type 1 | (Orphanet:812) |
Spinocerebellar ataxia type 19/22 | (Orphanet:98772) |
Spinocerebellar ataxia with epilepsy | (Orphanet:254881) |
X-linked sideroblastic anemia - ataxia | (Orphanet:2802) |
X-linked spastic paraplegia type 34 | (Orphanet:171607) |