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Q46035650-9F7E0CEA-7BEE-42D4-BD63-9486A6D112DE
Q46035650-9F7E0CEA-7BEE-42D4-BD63-9486A6D112DE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q46035650-9F7E0CEA-7BEE-42D4-BD63-9486A6D112DE
Congenital disorder of glycosylation type Ia: heterogeneity in the clinical presentation from multivisceral failure to hyperinsulinaemic hypoglycaemia as leading symptoms in three infants with phosphomannomutase deficiency.
P2860
Q46035650-9F7E0CEA-7BEE-42D4-BD63-9486A6D112DE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q46035650-9F7E0CEA-7BEE-42D4-BD63-9486A6D112DE
rank
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type
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wasDerivedFrom
4a9c13e281243211b5700c4adfc71feae02eeb0b
P2860
Congenital disorder of glycosylation id presenting with hyperinsulinemic hypoglycemia and islet cell hyperplasia.