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Summary Literature (0)
DOID:0060285 - parietal foramina


Disease Ontology 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.

Synonyms: Caitlin marks, enlarged parietal foramina, hereditary cranium bifidum

Xenbase Genes : msx2, alx4

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0018953 - parietal foramina

OMIM:
OMIM:168500 - PARIETAL FORAMINA 1; PFM1
OMIM:609566 - PARIETAL FORAMINA 3; PFM3
OMIM:609597 - PARIETAL FORAMINA 2; PFM2

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): neural tube defect (is_a)