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Q46147309-E1282A23-2C97-4AF9-85E6-9FC6CDC33F5C
Q46147309-E1282A23-2C97-4AF9-85E6-9FC6CDC33F5C
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Statement
http://www.wikidata.org/entity/statement/Q46147309-E1282A23-2C97-4AF9-85E6-9FC6CDC33F5C
Apparent mineralocorticoid excess syndrome in a Brazilian boy caused by the homozygous missense mutation p.R186C in the HSD11B2 gene.
P2860
Q46147309-E1282A23-2C97-4AF9-85E6-9FC6CDC33F5C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q46147309-E1282A23-2C97-4AF9-85E6-9FC6CDC33F5C
rank
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type
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Statement
wasDerivedFrom
d0ab2b05b80c673e105720335431f2786a7ab824
P2860
Monogenic low renin hypertension.