Episodic ataxia

Symptom Information:

Symptom ID: HPO:0002131
Synonyms:
Episodic ataxia [OMIM:Episodic ataxia]
Ataxia, episodic [OMIM:Ataxia, episodic]
Ataxia, episodic (episodes last from hours to days) [OMIM:Ataxia, episodic (episodes last from hours to days)]
Quality:
Cross references:
OMIM: "Episodic ataxia" [OMIM:Episodic ataxia]
OMIM: "Ataxia, episodic" [OMIM:Ataxia, episodic]
OMIM: "Ataxia, episodic (episodes last from hours to days)" [OMIM:Ataxia, episodic (episodes last from hours to days)]
Is a (Direct Parents):
HPO         Ataxia
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:
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)