Episodic ataxia
Symptom Information:
Symptom ID: | HPO:0002131 | |||
Synonyms: |
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Quality: | ||||
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) Abnormality of coordination(HPO:0011443) Ataxia(HPO:0001251) Episodic ataxia(HPO:0002131) MedDRA: |
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Database Frequency: | 16 / 7739 | |||
Resource: |
All diseases associated with this symptom:
Benign paroxysmal tonic upgaze of childhood with ataxia | (Orphanet:1179) |
CEREBELLAR ATAXIA, AREFLEXIA, PES CAVUS, OPTIC ATROPHY, AND SENSORINEURALHEARING LOSS | (OMIM:601338) |
EPISODIC ATAXIA, TYPE 8 | (OMIM:616055) |
Episodic ataxia type 1 | (Orphanet:37612) |
Episodic ataxia type 3 | (Orphanet:79135) |
Episodic ataxia type 4 | (Orphanet:79136) |
Episodic ataxia type 5 | (Orphanet:211067) |
Episodic ataxia type 6 | (Orphanet:209967) |
Episodic ataxia type 7 | (Orphanet:209970) |
Familial paroxysmal ataxia | (Orphanet:97) |
Hartnup syndrome | (Orphanet:2116) |
Hereditary continuous muscle fiber activity | (Orphanet:972) |
MIGRAINE, FAMILIAL HEMIPLEGIC, 2 | (OMIM:602481) |
Ornithine transcarbamylase deficiency | (Orphanet:664) |
Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity | (Orphanet:53583) |
Pyruvate dehydrogenase E1-alpha deficiency | (Orphanet:79243) |