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:
Neoplasm of the adrenal cortex (HP:0100641)

Parent Node:
Adrenocortical adenoma (HP:0008256)

..Starting node
..Non-secretory adrenocortical adenoma (HP:0011745)

Term ID:

11745

Name:

Non-secretory adrenocortical adenoma

Synonym:

Non-secretory adrenal adenoma

Definition:

An hormonally inactive adrenocortical adenoma, that is, an adenoma that does not secrete excessive amounts of adrenal hormones.

Comments:

Reference:

HP:0011745

Genes and Diseases:

Child Nodes:

Sister Nodes:

Secretory adrenocortical adenoma (HP:0011746)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011745	HP:0011745	Non-secretory adrenocortical adenoma	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.