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Reference

Evidence

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Outcomes
Proteins
Interactions
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Articles

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Reach

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Processes
Anatomy
Cell types
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Materials
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Diseases

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craniosynostosis 7

MONDO:0044315Mondo

Open in the graph

Findings

No curated finding names craniosynostosis 7 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.

Genes

1 gene

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.

SMAD6HGNC:6772
- Strong · PanelApp Australia · Autosomal dominant · 2025
- Moderate · Ambry Genetics · Autosomal dominant · 2022
- Limited · Labcorp Genetics (formerly Invitae) · Unknown · 2023
- Limited · G2P · Autosomal dominant · 2019

Where it sits

A kind of: inherited disease susceptibility
SMAD6-related disease

Other names

1 name

Resolves to: craniosynostosis 7

Also called: craniosynostosis 7, susceptibility to