glycogen storage disease due to glucose-6-phosphatase deficiency type IB

Summary

glycogen storage disease due to glucose-6-phosphatase deficiency type IB is a class of disease^[1].

Key Facts

• glycogen storage disease due to glucose-6-phosphatase deficiency type IB's instance of is recorded as class of disease^[2].
• glycogen storage disease due to glucose-6-phosphatase deficiency type IB's subclass of is recorded as glycogen storage disease due to glucose-6-phosphatase deficiency^[3].
• glycogen storage disease due to glucose-6-phosphatase deficiency type IB's MeSH descriptor ID is recorded as C562594^[4].
• glycogen storage disease due to glucose-6-phosphatase deficiency type IB's OMIM ID is recorded as 232220^[5].
• glycogen storage disease due to glucose-6-phosphatase deficiency type IB's Orphanet ID is recorded as 79259^[6].
• glycogen storage disease due to glucose-6-phosphatase deficiency type IB's NCI Thesaurus ID is recorded as C122661^[7].
• glycogen storage disease due to glucose-6-phosphatase deficiency type IB's genetic association is recorded as SLC37A4^[8].
• glycogen storage disease due to glucose-6-phosphatase deficiency type IB's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_364^[9].
• glycogen storage disease due to glucose-6-phosphatase deficiency type IB's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_79259^[10].
• glycogen storage disease due to glucose-6-phosphatase deficiency type IB's UMLS CUI is recorded as C0268146^[11].
• glycogen storage disease due to glucose-6-phosphatase deficiency type IB's ICD-10-CM is recorded as E74.0^[12].
• glycogen storage disease due to glucose-6-phosphatase deficiency type IB's GARD rare disease ID is recorded as 2515^[13].
• glycogen storage disease due to glucose-6-phosphatase deficiency type IB's Mondo ID is recorded as MONDO_0009288^[14].
• glycogen storage disease due to glucose-6-phosphatase deficiency type IB's UniProt disease ID is recorded as DI-00519^[15].