Fraser Syndrome 2 C4540036
A genetic form of Fraser syndrome causing similar multi-system abnormalities affecting eyes, ears, kidneys, and other organs. Treatment is supportive and addresses individual complications.
Key facts at a glance
- ICD-10
- Q89.9
- ICD-11
- LA00.0
- Body system
- congenital
- Severity
- severe
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Warning signs - seek immediate care
Cryptophthalmos
Diaphragmatic hernia
Tracheoesophageal fistula
Generalized symptoms
(congenital)Significant symptoms that substantially affect daily functioning.
Frequency: Common at all stages
Syndactyly
(musculoskeletal)Medication Comparisons
Compare medications used to treat Fraser Syndrome 2 C4540036. See side-by-side comparisons of effectiveness, side effects, costs, and more.
View Medication ComparisonsThis information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy