Waardenburg syndrome type 3

Summary

Waardenburg syndrome type 3 is a rare disease^[1].

Key Facts

• Waardenburg syndrome type 3's instance of is recorded as rare disease^[2].
• Waardenburg syndrome type 3's instance of is recorded as class of disease^[3].
• Waardenburg syndrome type 3's subclass of is recorded as Waardenburg's syndrome^[4].
• Waardenburg syndrome type 3's OMIM ID is recorded as 148820^[5].
• Waardenburg syndrome type 3's Disease Ontology ID is recorded as DOID:0110949^[6].
• Waardenburg syndrome type 3's Orphanet ID is recorded as 896^[7].
• Waardenburg syndrome type 3's genetic association is recorded as PAX3^[8].
• Waardenburg syndrome type 3's Google Knowledge Graph ID is recorded as /g/11j19y_86z^[9].
• Waardenburg syndrome type 3's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110949^[10].
• Waardenburg syndrome type 3's exact match is recorded as http://identifiers.org/doid/DOID:0110949^[11].
• Waardenburg syndrome type 3's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_896^[12].
• Waardenburg syndrome type 3's UMLS CUI is recorded as C0079661^[13].
• Waardenburg syndrome type 3's ICD-10-CM is recorded as E70.3^[14].
• Waardenburg syndrome type 3's GARD rare disease ID is recorded as 5523^[15].
• Waardenburg syndrome type 3's on focus list of Wikimedia project is recorded as WikiProject Medicine^[16].
• Waardenburg syndrome type 3's Mondo ID is recorded as MONDO_0007862^[17].
• Waardenburg syndrome type 3's ICD-11 ID is recorded as 847608197^[18].
• Waardenburg syndrome type 3's UniProt disease ID is recorded as DI-01138^[19].