Wolfram syndrome 1

Summary

Wolfram syndrome 1 is a class of disease^[1].

Key Facts

• Wolfram syndrome 1's instance of is recorded as class of disease^[2].
• Wolfram syndrome 1's subclass of is recorded as Wolfram syndrome^[3].
• Wolfram syndrome 1's subclass of is recorded as autosomal recessive disease^[4].
• Wolfram syndrome 1's part of is recorded as Wolfram syndrome^[5].
• Wolfram syndrome 1's OMIM ID is recorded as 222300^[6].
• Wolfram syndrome 1's afflicts is recorded as Homo sapiens^[7].
• Wolfram syndrome 1's Disease Ontology ID is recorded as DOID:0110629^[8].
• Wolfram syndrome 1's genetic association is recorded as WFS1^[9].
• Wolfram syndrome 1's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110629^[10].
• Wolfram syndrome 1's exact match is recorded as http://identifiers.org/doid/DOID:0110629^[11].
• Wolfram syndrome 1's UMLS CUI is recorded as CL1919860^[12].
• Wolfram syndrome 1's ICD-10-CM is recorded as E13.8^[13].
• Wolfram syndrome 1's on focus list of Wikimedia project is recorded as WikiProject Medicine^[14].
• Wolfram syndrome 1's Mondo ID is recorded as MONDO_0009101^[15].
• Wolfram syndrome 1's UniProt disease ID is recorded as DI-01151^[16].