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Disease Ontology Browser
parietal foramina (DOID:0060285)
Alliance: disease page
Synonyms: Caitlin marks; enlarged parietal foramina; hereditary cranium bifidum
Alt IDs: OMIM:168500, OMIM:609566, OMIM:609597, MESH:C566826, ORDO:60015, UMLS_CUI:C1868598
Definition: 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.

Disease References using Mouse Models (2)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/17/2024
MGI 6.24 		The Jackson Laboratory