parietal foramina 2
MONDO:0012309Mondo
Findings
No curated finding names parietal foramina 2 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any parietal foramina in which the cause of the disease is a mutation in the ALX4 gene.
Definition from the Mondo Disease Ontology (MONDO:0012309), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Congenital onset
HPO, annotations 2026-09-02
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.
- ALX4HGNC:450
- Definitive · G2P · Autosomal dominant · 2025
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2021
- Strong · PanelApp Australia · Autosomal dominant · 2025
- Moderate · Ambry Genetics · Autosomal dominant · 2018
Where it sits
- A kind of
Other names
3 names
Resolves to: parietal foramina 2
- Also called
- ALX4 parietal foraminaparietal foramina caused by mutation in ALX4parietal foramina type 2