Perry syndrome
Human disease
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Perry syndrome
Summary
Perry syndrome is a designated intractable/rare disease[1]. It is known by 5 alternative names across languages and contexts.[2]
Key Facts
- Perry syndrome's instance of is recorded as designated intractable/rare disease[3].
- Perry syndrome's instance of is recorded as rare disease[4].
- Perry syndrome's instance of is recorded as class of disease[5].
- Perry syndrome is a type of syndrome[6].
- Perry syndrome is a type of rare parkinsonian syndrome due to genetic neurodegenerative disease[7].
- Perry syndrome is a type of genetic disease[8].
- Perry syndrome is a type of autosomal dominant disease[9].
- Perry syndrome's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4702[10].
- Perry syndrome's ICD-9-CM is recorded as 348.89[11].
- Perry syndrome's genetic association is recorded as DCTN1[12].
- Perry syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060486[13].
- Perry syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060486[14].
- Perry syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_178509[15].
- Perry syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
Why It Matters
Perry syndrome is known by 5 alternative names across languages and contexts.[2]