glycogen storage disease due to glucose-6-phosphatase deficiency type Ia
Glycogenosis due to glucose-6-phosphatase deficiency (G6P) type a, or glycogen storage disease (GSD) type 1a, is a type of glycogenosis due to G6P deficiency (see this term)
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glycogen storage disease due to glucose-6-phosphatase deficiency type Ia
Summary
glycogen storage disease due to glucose-6-phosphatase deficiency type Ia is a class of disease[1].
Key Facts
- glycogen storage disease due to glucose-6-phosphatase deficiency type Ia's instance of is recorded as class of disease[2].
- glycogen storage disease due to glucose-6-phosphatase deficiency type Ia'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 Ia's OMIM ID is recorded as 232200[4].
- glycogen storage disease due to glucose-6-phosphatase deficiency type Ia's Orphanet ID is recorded as 79258[5].
- glycogen storage disease due to glucose-6-phosphatase deficiency type Ia's NCI Thesaurus ID is recorded as C162398[6].
- glycogen storage disease due to glucose-6-phosphatase deficiency type Ia's genetic association is recorded as G6PC1[7].
- glycogen storage disease due to glucose-6-phosphatase deficiency type Ia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_364[8].
- glycogen storage disease due to glucose-6-phosphatase deficiency type Ia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_79258[9].
- glycogen storage disease due to glucose-6-phosphatase deficiency type Ia's UMLS CUI is recorded as C0017920[10].
- glycogen storage disease due to glucose-6-phosphatase deficiency type Ia's UMLS CUI is recorded as C2919796[11].
- glycogen storage disease due to glucose-6-phosphatase deficiency type Ia's UMLS CUI is recorded as CN069618[12].
- glycogen storage disease due to glucose-6-phosphatase deficiency type Ia's UMLS CUI is recorded as C5680202[13].
- glycogen storage disease due to glucose-6-phosphatase deficiency type Ia's ICD-10-CM is recorded as E74.0[14].
- glycogen storage disease due to glucose-6-phosphatase deficiency type Ia's GARD rare disease ID is recorded as 7864[15].
- glycogen storage disease due to glucose-6-phosphatase deficiency type Ia's Mondo ID is recorded as MONDO_0009287[16].
- glycogen storage disease due to glucose-6-phosphatase deficiency type Ia's UniProt disease ID is recorded as DI-00518[17].