Kisho is an information platform, not a medical provider. Nothing on this site constitutes medical advice, diagnosis, or treatment recommendations. All content is aggregated from publicly available sources (including ClinicalTrials.gov, PubMed, FDA.gov, and Orphanet) and is provided for informational purposes only. Clinical trial eligibility, treatment decisions, and any health-related actions should always be discussed with a qualified healthcare professional. Kisho does not endorse any specific therapy, organization, or clinical trial. Terms of use · Privacy policy
Features include: Congenital diaphragmatic hernia.
Organ System | Phenotype Count | Example Features |
|---|---|---|
Pregnancy and birth | 1 | Congenital diaphragmatic hernia |
PLS3 function has not been fully characterized.
Hernia, anterior diaphragmatic is associated with mutations in the PLS3 gene on chromosome X.
Genetic testing for PLS3 is available. Testing is considered confirmatory for diagnosis.
No clinical trials have been registered for hernia, anterior diaphragmatic.
1 publication has been identified in PubMed for hernia, anterior diaphragmatic. Research spans Case Report / Case Series (100%).
Lo Presti F (2024). [PMID: 39037933](https://pubmed.ncbi.nlm.nih.gov/39037933/). *Interdisciplinary cardiovascular and thoracic surgery*. [Case Report / Case Series]
Data assembled from 5 of 12 sources · Last updated Sep 19, 2026, 10:42 PM UTC
Online Mendelian Inheritance in Man
Genetic and Rare Diseases Info Center