Usher syndrome type 2D

Summary

Usher syndrome type 2D is a rare disease^[1].

Key Facts

• Usher syndrome type 2D's instance of is recorded as rare disease^[2].
• Usher syndrome type 2D's instance of is recorded as class of disease^[3].
• Usher syndrome type 2D's subclass of is recorded as Usher syndrome type 2^[4].
• Usher syndrome type 2D's OMIM ID is recorded as 611383^[5].
• Usher syndrome type 2D's OMIM ID is recorded as 611383^[6].
• Usher syndrome type 2D's Disease Ontology ID is recorded as DOID:0110840^[7].
• Usher syndrome type 2D's genetic association is recorded as WHRN^[8].
• Usher syndrome type 2D's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110840^[9].
• Usher syndrome type 2D's exact match is recorded as http://identifiers.org/doid/DOID:0110840^[10].
• Usher syndrome type 2D's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_231178^[11].
• Usher syndrome type 2D's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_886^[12].
• Usher syndrome type 2D's UMLS CUI is recorded as C1568249^[13].
• Usher syndrome type 2D's ICD-10-CM is recorded as H35.5^[14].
• Usher syndrome type 2D's on focus list of Wikimedia project is recorded as WikiProject Medicine^[15].
• Usher syndrome type 2D's Mondo ID is recorded as MONDO_0012662^[16].
• Usher syndrome type 2D's UniProt disease ID is recorded as DI-02406^[17].