Stickler syndrome type 2

Summary

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

Key Facts

• Stickler syndrome type 2's instance of is recorded as class of disease^[2].
• Stickler syndrome type 2's subclass of is recorded as Stickler syndrome^[3].
• Stickler syndrome type 2's subclass of is recorded as autosomal dominant disease^[4].
• Stickler syndrome type 2's MeSH descriptor ID is recorded as C537493^[5].
• Stickler syndrome type 2's OMIM ID is recorded as 604841^[6].
• Stickler syndrome type 2's Disease Ontology ID is recorded as DOID:0080675^[7].
• Stickler syndrome type 2's Orphanet ID is recorded as 90654^[8].
• Stickler syndrome type 2's NCI Thesaurus ID is recorded as C74985^[9].
• Stickler syndrome type 2's genetic association is recorded as COL11A1^[10].
• Stickler syndrome type 2's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_828^[11].
• Stickler syndrome type 2's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_90654^[12].
• Stickler syndrome type 2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080675^[13].
• Stickler syndrome type 2's exact match is recorded as http://identifiers.org/doid/DOID:0080675^[14].
• Stickler syndrome type 2's UMLS CUI is recorded as C1858084^[15].
• Stickler syndrome type 2's ICD-10-CM is recorded as Q87.5^[16].
• Stickler syndrome type 2's GARD rare disease ID is recorded as 5020^[17].
• Stickler syndrome type 2's Mondo ID is recorded as MONDO_0011493^[18].
• Stickler syndrome type 2's UniProt disease ID is recorded as DI-01092^[19].