(Q56014440)

English

familial hyperreninemic hypoaldosteronism type 1

human disease

FHHA1
CMO I
Aldosterone synthase deficiency
CMO II
Corticosterone methyloxidase deficiency type I
18-hydroxylase deficiency
18-oxidase deficiency

In more languages

Statements

class of disease

0 references

familial hypoaldosteronism

1 reference

Monarch Disease Ontology release 2018-06-29

7 August 2018

http://www.orpha.net/ORDO/Orphanet_99763

0 references

Identifiers

0 references

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

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

7 August 2018

Sitelinks

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