> Trialight public data. Index of pages: https://trialight.com/llms.txt
> Web page: https://trialight.com/data/condition/congenital-d1a6f843-40e2-5921-8397-b0ddf98525b7
> Record changed: 2026-10-13

# Congenital

Rare disease

No

## Definition and classification

**Definition**

A characteristic of a disease in which the disease is present at birth, regardless of cause.

**Genetic basis**

No

**Non-human condition**

No

**Rare disease**

No

**Listing at source**

Listed

**Condition name**

Congenital

### Alternative names (2)

- congenital
- inborn

## Clinical profile

**Severity**

Unknown

## Identifiers

**MONDO ID**

MONDO:0021140

Source: [monarchinitiative.org](https://monarchinitiative.org/MONDO:0021140)

**Parent condition**

MONDO:0021139

## Related records

### Broader conditions (2)

- Congenital or acquired
- Disease characteristic

### Trials (770)

- 'TOTAL' (Tracheal Occlusion To Accelerate Lung Growth) Trial
- "Evaluation of Clinical and Radiographic Results of Pseudarthrosis of Clavicle Treated With Plaque and Screws"
- 3D Animation and Models to Aid Management of Fetal CDH
- 4D-310 in Adults With Fabry Disease and Cardiac Involvement
- A 2-Period Crossover Study of BPN14770 in Adults Males With Fragile X Syndrome
- A Clinical Investigation of the C2a-Taper™ Acetabular System
- A Clinical Trial Study of Hip System in Primary Total Hip Arthroplasty in China
- A Clinical Trial to Evaluate the Safety and Efficacy of BMN 111 in Infants and Young Children With Achondroplasia
- A Comparative Analysis of Speech Perception Between Cochlear Implant Patients and DFNB9 Patients Receiving Gene Therapy
- A Comprehensive Approach To Relief Of Digestive Symptoms In Cystic Fibrosis: CARDS-CF
- A Gene Therapy Study for Homozygous Familial Hypercholesterolemia (HoFH)
- A Gene Transfer Study for Hemophilia A
- A Long-term Follow-up Study in Participants Who Received CTX001
- A Long-Term Follow-Up Study in Severe Hemophilia A Subjects Who Received BMN 270 in a Prior BioMarin Clinical Trial (270-401)
- A Long-Term Follow-Up Study of Participants With Sickle Cell Disease or Transfusion Dependent β-Thalassemia Who Received EDIT-301
- A Long-term Follow-up Study to Evaluate the Safety and Efficacy of RGX-501
- A Long-Term Observational Study of Patients With Fucosidosis
- A Multi-Centre Study in Patients Undergoing Total Hip Arthroplasty With the Smith+Nephew CATALYSTEM™ Primary Hip System
- A Multi-centre Study to Assess the Long-term Performance of the DePuy ASR™ System in Primary Hip Resurfacing Surgery
- A Multi-centre Study to Assess the Long-term Performance of the DePuy PROXIMA™ Hip in Primary Total Hip Replacement

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