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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:0018953 - parietal foramina |
| MIM:168500 - PARIETAL FORAMINA 1; PFM1 |
| MIM:609566 - PARIETAL FORAMINA 3; PFM3 |
| MIM:609597 - PARIETAL FORAMINA 2; PFM2 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
neural tube defect (is_a)