Trait
Abnormality of the abdominal wall
Clinical name: Abnormal abdominal wall morphology
The presence of any abnormality affecting the abdominal wall.
Summary
- Also called
- Abnormality of external features of the abdomen
- Body system
- Abnormality of the digestive 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/abnormal-abdominal-wall-morphology.json"
page <- fromJSON(url)
page$trait$nameRead the genes linked to Abnormality of the abdominal wall, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome Test8 condition reports read genes linked to this trait
Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.
- 3MC Syndrome 1 (MASP1)Reads 1 of these genesMASP1About this report →
- CTNNB1 SyndromeReads 1 of these genesCTNNB1About this report →
- Spondyloepiphyseal Dysplasia With Congenital Joint DislocationsReads 1 of these genesCHST3About this report →
- Colorectal Cancer & PolyposisReads 1 of these genesAPCAbout this report →
Show 4 more reports
Read the genes linked to Abnormality of the abdominal wall, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome Test9 genes linked to Abnormality of the abdominal wall
Changes in these genes cause rare conditions in which Abnormality of the abdominal wall 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 |
|---|---|---|
| APCAPC regulator of Wnt signaling pathway | Very often (80–99%) | In 1 condition |
| CTNNB1catenin beta 1 | Very often (80–99%) | In 1 condition |
| STSsteroid sulfatase | Sometimes (5–29%) | In 1 condition |
| USP9Xubiquitin specific peptidase 9 X-linked | Sometimes (5–29%) | In 1 condition |
| B3GAT3beta-1,3-glucuronyltransferase 3 | Not recorded | In 1 condition |
| CHST3carbohydrate sulfotransferase 3 | Not recorded | In 1 condition |
| HLA-DQA1major histocompatibility complex, class II, DQ alpha 1 | Not recorded | In 1 condition |
| HLA-DQB1major histocompatibility complex, class II, DQ beta 1 | Not recorded | In 1 condition |
| MASP1MBL associated serine protease 1 | 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 2026.10.19-9814e911.
From traits to your genome
Read the genes behind these traits in your own DNA.
The Genome Test sequences nearly all of your DNA, not a preset panel, so every gene on these pages is in your data. Premium adds 810+ physician-ready reports.
Free shipping · Results in 6–8 weeks
