XFE progeroid syndrome

Summary

XFE progeroid syndrome is a rare disease^[1].

Key Facts

• XFE progeroid syndrome's instance of is recorded as rare disease^[2].
• XFE progeroid syndrome's instance of is recorded as class of disease^[3].
• XFE progeroid syndrome's subclass of is recorded as syndrome^[4].
• XFE progeroid syndrome's subclass of is recorded as progeroid syndrome^[5].
• XFE progeroid syndrome's subclass of is recorded as genetic disease^[6].
• XFE progeroid syndrome's subclass of is recorded as autosomal recessive disease^[7].
• XFE progeroid syndrome's MeSH descriptor ID is recorded as C567043^[8].
• XFE progeroid syndrome's OMIM ID is recorded as 610965^[9].
• XFE progeroid syndrome's Disease Ontology ID is recorded as DOID:0060590^[10].
• XFE progeroid syndrome's NCI Thesaurus ID is recorded as C173111^[11].
• XFE progeroid syndrome's genetic association is recorded as ERCC4^[12].
• XFE progeroid syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060590^[13].
• XFE progeroid syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060590^[14].
• XFE progeroid syndrome's UMLS CUI is recorded as C1970416^[15].
• XFE progeroid syndrome's GARD rare disease ID is recorded as 10628^[16].
• XFE progeroid syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine^[17].
• XFE progeroid syndrome's Mondo ID is recorded as MONDO_0012590^[18].
• XFE progeroid syndrome's UniProt disease ID is recorded as DI-02464^[19].