/parietal foramina 1

parietal foramina 1

Rare Disease

MONDO:0008197

Also Known As

MSX2 parietal foraminaparietal foramina 1parietal foramina caused by mutation in MSX2PFMPFM1catlin Markscranium bifidum occultumcranium bifidum, hereditaryforamina parietalia permagnaparietal foraminaparietal foramina, symmetric

Definition

Any parietal foramina in which the cause of the disease is a mutation in the MSX2 gene.

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

Checking for content...

Associated Genes

MSX2 ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:168500 ↗

GARD

GARD:18051 ↗

Related Diseases

parietal foramina 3

MONDO:0012302

Rare

parietal foramina 2

MONDO:0012309

Rare

← Back to All Diseases