Cornelia de Lange syndrome 1

Findings

No curated finding names Cornelia de Lange syndrome 1 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

Congenital onset · Infantile 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 1

Also called

Cornelia de Lange syndrome caused by mutation in NIPBLCornelia De Lange syndrome type 1NIPBL Cornelia de Lange syndrome