glycogen storage disease IXb
Glycogen storage disease (GSD) due to liver and muscle phosphorylase kinase (PhK) deficiency is a benign inborn error of glycogen metabolism. It is the mildest form of GSD due to PhK deficiency (see this term).
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glycogen storage disease IXb
Summary
glycogen storage disease IXb is a rare disease[1]. It is known by 15 alternative names across languages and contexts.[2]
Key Facts
- glycogen storage disease IXb's instance of is recorded as rare disease[3].
- glycogen storage disease IXb's instance of is recorded as class of disease[4].
- glycogen storage disease IXb is a type of glycogen storage disease IX[5].
- glycogen storage disease IXb is a type of muscular glycogenosis[6].
- glycogen storage disease IXb is a type of rare metabolic liver disease[7].
- glycogen storage disease IXb is a type of genetic disease[8].
- glycogen storage disease IXb's symptoms and signs is recorded as left upper quadrant abdominal rigidity[9].
- glycogen storage disease IXb's genetic association is recorded as PHKB[10].
- glycogen storage disease IXb's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111041[11].
- glycogen storage disease IXb's exact match is recorded as http://identifiers.org/doid/DOID:0111041[12].
- glycogen storage disease IXb's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_79240[13].
- glycogen storage disease IXb's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
Why It Matters
glycogen storage disease IXb is known by 15 alternative names across languages and contexts.[2]