Cornelia de Lange syndrome 3

Findings

No curated finding names Cornelia de Lange syndrome 3 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.

Definition

Inheritance

Autosomal dominant inheritance

Onset and course

Infantile onset · Childhood onset

HPO, annotations 2026-09-02

What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.

Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.

Where it sits

A kind of

• Cornelia de Lange syndrome
• non-syndromic limb reduction defect

Resolves to: Cornelia de Lange syndrome 3

Also called

Cornelia de Lange syndrome caused by mutation in SMC3Cornelia De Lange syndrome type 3SMC3 Cornelia de Lange syndrome