Human Phenotype Ontology

Hello! Guest! Please Login or Register! Clinician Mode

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:
Abnormality of the adrenal glands (HP:0000834)

Parent Node:
Abnormality of adrenal morphology (HP:0011732)

..Starting node
..Ectopic adrenal gland (HP:0011742)

Term ID:

11742

Name:

Ectopic adrenal gland

Synonym:

Abnormal adrenal gland position

Definition:

Abnormal anatomical location of the adrenal gland.

Comments:

Reference:

HP:0011742

Genes and Diseases:

Child Nodes:

Sister Nodes:

Adrenal calcification (HP:0010512)

Adrenal gland dysgenesis (HP:0008216)

Adrenal hyperplasia (HP:0008221)

Adrenal hypoplasia (HP:0000835)

Adrenocortical abnormality (HP:0000849)

Adrenocortical cytomegaly (HP:0008186)

Neoplasm of the adrenal gland (HP:0100631)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011742	HP:0011742	Ectopic adrenal gland	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.