Usher syndrome type 2A

Summary

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

Key Facts

• Usher syndrome type 2A's instance of is recorded as rare disease^[2].
• Usher syndrome type 2A's instance of is recorded as class of disease^[3].
• Usher syndrome type 2A's subclass of is recorded as Usher syndrome type 2^[4].
• Usher syndrome type 2A's MeSH descriptor ID is recorded as C536490^[5].
• Usher syndrome type 2A's OMIM ID is recorded as 276901^[6].
• Usher syndrome type 2A's Disease Ontology ID is recorded as DOID:0110838^[7].
• Usher syndrome type 2A's genetic association is recorded as PDZD7^[8].
• Usher syndrome type 2A's genetic association is recorded as USH2A^[9].
• Usher syndrome type 2A's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110838^[10].
• Usher syndrome type 2A's exact match is recorded as http://identifiers.org/doid/DOID:0110838^[11].
• Usher syndrome type 2A's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_231178^[12].
• Usher syndrome type 2A's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_886^[13].
• Usher syndrome type 2A's UMLS CUI is recorded as C1848634^[14].
• Usher syndrome type 2A's ICD-10-CM is recorded as H35.5^[15].
• Usher syndrome type 2A's GARD rare disease ID is recorded as 5440^[16].
• Usher syndrome type 2A's on focus list of Wikimedia project is recorded as WikiProject Medicine^[17].
• Usher syndrome type 2A's Mondo ID is recorded as MONDO_0010169^[18].
• Usher syndrome type 2A's UniProt disease ID is recorded as DI-01118^[19].