Parietal Foramina (FPP)

Alias:

Enlarged Parietal Foramina

Symmetric Parietal Foramina

Hereditary Cranium Bifidum

Foramina Parietalia Permagna

Catlin Marks

Fenestrae Parietales Symmetricae

Fenestrae Parietals Symmetricae

Cranium Bifidum Occultum

Giant Parietal Foramina

Cranium Bifidum

Caitlin Marks

Pfm

Fpp

Favorite

Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Parietal Foramina, also known as enlarged parietal foramina, is related to parietal foramina with cleidocranial dysplasia and potocki-shaffer syndrome. An important gene associated with Parietal Foramina is MSX2 (Msh Homeobox 2), and among its related pathways/superpathways are Neural crest differentiation and 11p11.2 copy number variation syndrome. Affiliated tissues include bone and brain, and related phenotypes are parietal foramina and vomiting

Related ID：

MALACARDS：PRT042

MESH：C566826