Trait
Enlarged adrenal glands
Clinical name: Adrenal hyperplasia
Enlargement of the adrenal gland.
Summary
- Body system
- Abnormality of the endocrine system
This page as data
Add .json to the page's address, or ask for application/json, to read it as JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/adrenal-hyperplasia.json"
page <- fromJSON(url)
page$trait$nameRead the genes linked to Enlarged adrenal glands, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome Test22 genes linked to Enlarged adrenal glands
Changes in these genes cause rare conditions in which Enlarged adrenal glands is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.
| Gene | How often it is seen | Conditions |
|---|---|---|
| AIREautoimmune regulator | Very often (80–99%) | In 1 condition |
| KCNJ5potassium inwardly rectifying channel subfamily J member 5 | Very often (80–99%) | In 2 conditions |
| ATRXATRX chromatin remodeler | Often (30–79%) | In 1 condition |
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Often (30–79%) | In 1 condition |
| CDH23cadherin related 23 | Often (30–79%) | In 1 condition |
| CYP11B1cytochrome P450 family 11 subfamily B member 1 | Often (30–79%) | In 2 conditions |
| CYP11B2cytochrome P450 family 11 subfamily B member 2 | Often (30–79%) | In 1 condition |
| NR3C1nuclear receptor subfamily 3 group C member 1 | Often (30–79%) | In 2 conditions |
| PORcytochrome p450 oxidoreductase | Often (30–79%) | In 1 condition |
| TP53tumor protein p53 | Often (30–79%) | In 1 condition |
| USP48ubiquitin specific peptidase 48 | Often (30–79%) | In 1 condition |
| USP8ubiquitin specific peptidase 8 | Often (30–79%) | In 1 condition |
| CLCN2chloride voltage-gated channel 2 | Sometimes (5–29%) | In 1 condition |
| ATP6V1B2ATPase H+ transporting V1 subunit B2 | Rarely (1–4%) | In 1 condition |
| CACNA1Dcalcium voltage-gated channel subunit alpha1 D | Rarely (1–4%) | In 1 condition |
| TBC1D24TBC1 domain family member 24 | Rarely (1–4%) | In 1 condition |
| CYP17A1cytochrome P450 family 17 subfamily A member 1 | Not recorded | In 1 condition |
| CYP21A2cytochrome P450 family 21 subfamily A member 2 | Not recorded | In 1 condition |
| GNASGNAS complex locus | Not recorded | In 1 condition |
| HSD3B2hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2 | Not recorded | In 1 condition |
| PDE8Bphosphodiesterase 8B | Not recorded | In 1 condition |
| PRKACAprotein kinase cAMP-activated catalytic subunit alpha | Not recorded | In 1 condition |
How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.
Narrower traits
Broader traits
Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks