Oculogyric crisis
Symptom Information:
Symptom ID: | HPO:0010553 | ||||
Synonyms: |
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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) Dystonia(HPO:0001332) Oculogyric crisis(HPO:0010553) MedDRA: Eye disorders(MedDRA:10015919) Ocular neuromuscular disorders(MedDRA:10030061) Ocular nerve and muscle disorders(MedDRA:10030059) Oculogyric crisis(HPO:0010553) |
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Database Frequency: | 5 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
6-pyruvoyl-tetrahydropterin synthase deficiency | (Orphanet:13) |
Aromatic L-amino acid decarboxylase deficiency | (Orphanet:35708) |
Autosomal recessive dopa-responsive dystonia | (Orphanet:101150) |
Dopa-responsive dystonia due to sepiapterin reductase deficiency | (Orphanet:70594) |
GTP cyclohydrolase I deficiency | (Orphanet:2102) |