Perry syndrome
Human disease
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Summary
Perry syndrome is a designated intractable/rare disease[1]. It is known by 5 alternative names across languages and contexts.[2]
Key Facts
- Instance of: rare disease[3], class of disease[4]
- Subclass of: syndrome[5], rare parkinsonian syndrome due to genetic neurodegenerative disease[6], genetic disease[7], autosomal dominant disease[8]
- Prevalence: 0.000001[9]
- External data available at URL: http://www.nanbyou.or.jp/entry/4702[10]
- ICD-9-CM: 348.89[11]
- Genetic association: DCTN1[12]
- Age of onset: adult onset[13]
- Exact match: http://purl.obolibrary.org/obo/DOID_0060486[14], http://identifiers.org/doid/DOID:0060486[15], http://www.orpha.net/ORDO/Orphanet_178509[16]
- On focus list of Wikimedia project: WikiProject Medicine[17]
- Has phenotype: weight loss[18], basal ganglia disease[19], sleep disturbance[20], Q141815669[21], respiratory arrest[22], dementia[23], personality change[24], hypotension[25], suicidal ideation[26]
- P14914: D178509[27]