(Q56014286)

English

autosomal recessive hyperinsulinism due to Kir6.2 deficiency

human disease

Autosomal recessive hyperinsulinemic hypoglycemia due to Kir6.2 deficiency

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Statements

class of disease

0 references

http://www.orpha.net/ORDO/Orphanet_79644

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Identifiers

1 reference

Monarch Disease Ontology release 2018-06-29

7 August 2018

0 references

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

7 August 2018

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