TMEM199-CDG

Summary

TMEM199-CDG is a rare disease^[1].

Key Facts

• TMEM199-CDG's instance of is recorded as rare disease^[2].
• TMEM199-CDG's instance of is recorded as class of disease^[3].
• TMEM199-CDG's subclass of is recorded as disorder of multiple glycosylation^[4].
• TMEM199-CDG's subclass of is recorded as rare hypercholesterolemia^[5].
• TMEM199-CDG's subclass of is recorded as congenital disorder of glycosylation type II^[6].
• TMEM199-CDG's subclass of is recorded as autosomal recessive disease^[7].
• TMEM199-CDG's OMIM ID is recorded as 616829^[8].
• TMEM199-CDG's Disease Ontology ID is recorded as DOID:0070268^[9].
• TMEM199-CDG's Orphanet ID is recorded as 466703^[10].
• TMEM199-CDG's genetic association is recorded as TMEM199^[11].
• TMEM199-CDG's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_466703^[12].
• TMEM199-CDG's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0070268^[13].
• TMEM199-CDG's UMLS CUI is recorded as C4225190^[14].
• TMEM199-CDG's on focus list of Wikimedia project is recorded as WikiProject Medicine^[15].
• TMEM199-CDG's Mondo ID is recorded as MONDO_0014790^[16].
• TMEM199-CDG's UniProt disease ID is recorded as DI-04627^[17].