Wolfram syndrome 2

Summary

Wolfram syndrome 2 is a class of disease^[1].

Key Facts

• Wolfram syndrome 2's instance of is recorded as class of disease^[2].
• Wolfram syndrome 2's subclass of is recorded as Wolfram syndrome^[3].
• Wolfram syndrome 2's subclass of is recorded as autosomal recessive disease^[4].
• Wolfram syndrome 2's part of is recorded as Wolfram syndrome^[5].
• Wolfram syndrome 2's MeSH descriptor ID is recorded as C565733^[6].
• Wolfram syndrome 2's OMIM ID is recorded as 604928^[7].
• Wolfram syndrome 2's afflicts is recorded as Homo sapiens^[8].
• Wolfram syndrome 2's Disease Ontology ID is recorded as DOID:0110630^[9].
• Wolfram syndrome 2's symptoms and signs is recorded as bleeding^[10].
• Wolfram syndrome 2's genetic association is recorded as CISD2^[11].
• Wolfram syndrome 2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110630^[12].
• Wolfram syndrome 2's exact match is recorded as http://identifiers.org/doid/DOID:0110630^[13].
• Wolfram syndrome 2's UMLS CUI is recorded as C1858028^[14].
• Wolfram syndrome 2's UMLS CUI is recorded as CL1919861^[15].
• Wolfram syndrome 2's ICD-10-CM is recorded as E13.8^[16].
• Wolfram syndrome 2's on focus list of Wikimedia project is recorded as WikiProject Medicine^[17].
• Wolfram syndrome 2's Mondo ID is recorded as MONDO_0011502^[18].
• Wolfram syndrome 2's UniProt disease ID is recorded as DI-02423^[19].