Human Phenotype Ontology

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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Grandparent Node:
Adrenal overactivity (HP:0002717)

Parent Node:
Hyperaldosteronism (HP:0000859)

..Starting node
..Secondary hyperaldosteronism (HP:0011741)

Term ID:

11741

Name:

Secondary hyperaldosteronism

Synonym:

Hyperreninemic hyperaldosteronism

Definition:

A form of hyperaldosteronism caused by abnormally increased renin levels.

Comments:

Reference:

HP:0011741

Genes and Diseases:

Child Nodes:

Sister Nodes:

Primary hyperaldosteronism (HP:0011736)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011741	HP:0011741	Secondary hyperaldosteronism	0	CL E G H

Genes (0) :

Diseases (0) :

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.