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parietal foramina 1
Disease Summary
Associated Targets (2)
Tbio
2
Mondo Description Any parietal foramina in which the cause of the disease is a mutation in the MSX2 gene.
Uniprot Description Autosomal dominant disease characterized by oval defects of the parietal bones caused by deficient ossification around the parietal notch, which is normally obliterated during the fifth fetal month.
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 UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
OMIM:168500
MONDO:0008197
High level summary of knowledge for a disease, including descriptions and datasource references.