You are using an outdated browser. Please upgrade your browser to improve your experience.
parietal foramina
Disease Summary
Associated Targets (2)
Tbio
2
Mondo Description Enlarged parietal foramina (EPF) is a developmental defect, characterized by variable intramembranous ossification defects of the parietal bones, which is either asymptomatic, symptomatic (headaches, nausea, vomiting, intellectual disability) or associated with other pathologies.
Disease Ontology Description An inherited neural tube defect that is characterized by enlarged openings in the parietal bones of the skull, has_material_basis_in mutation in the ALX4 gene or MSX2 gene.
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
Description from Disease Ontology
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
DOID:0060285
MESH:C566826
OMIMPS:168500
Orphanet:60015
SCTID:718099006
MONDO:0018953
High level summary of knowledge for a disease, including descriptions and datasource references.