glycogen storage disease IXa
human disease
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Summary
glycogen storage disease IXa is a rare disease[1].
Key Facts
- glycogen storage disease IXa's instance of is recorded as rare disease[2].
- glycogen storage disease IXa's instance of is recorded as class of disease[3].
- glycogen storage disease IXa's subclass of is recorded as glycogen storage disease IX[4].
- glycogen storage disease IXa's subclass of is recorded as X-linked recessive disease[5].
- glycogen storage disease IXa's MeSH descriptor ID is recorded as C564421[6].
- glycogen storage disease IXa's OMIM ID is recorded as 306000[7].
- glycogen storage disease IXa's Disease Ontology ID is recorded as DOID:0111042[8].
- glycogen storage disease IXa's symptoms and signs is recorded as left upper quadrant abdominal rigidity[9].
- glycogen storage disease IXa's genetic association is recorded as PHKA2[10].
- glycogen storage disease IXa's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111042[11].
- glycogen storage disease IXa's exact match is recorded as http://identifiers.org/doid/DOID:0111042[12].
- glycogen storage disease IXa's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_264580[13].
- glycogen storage disease IXa's UMLS CUI is recorded as C1844412[14].
- glycogen storage disease IXa's UMLS CUI is recorded as C2748941[15].
- glycogen storage disease IXa's UMLS CUI is recorded as C1418533[16].
- glycogen storage disease IXa's UMLS CUI is recorded as C0017927[17].
- glycogen storage disease IXa's ICD-10-CM is recorded as E74.0[18].
- glycogen storage disease IXa's on focus list of Wikimedia project is recorded as WikiProject Medicine[19].
- glycogen storage disease IXa's Mondo ID is recorded as MONDO_0010598[20].
- glycogen storage disease IXa's UniProt disease ID is recorded as DI-00528[21].