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loading...| Preferred Name |
Parietal Foramina |
| Synonyms |
Cranium Bifidum, Hereditary |
| ID |
http://purl.bioontology.org/ontology/MESH/C566826 |
| altLabel |
Cranium Bifidum, Hereditary Enlarged Parietal Foramina Parietal Foramina, Symmetric Catlin Marks Foramina Parietalia Permagna Cranium Bifidum Occultum |
| cui |
C1868598 |
| HM |
D004677 |
| Inverse of RB |
0 |
| Mapped to | |
| MDA |
20121105 |
| MeSH Frequency |
40 |
| MMR |
20160929 |
| notation |
C566826 |
| prefLabel |
Parietal Foramina |
| SC |
3 |
| Scope Statement |
Abnormal, symmetric, oval openings in the PARIETAL BONE on each side of the sagittal suture and separated from each other by a narrow bridge of bone. Their size decreases with age and considerable intrafamilial variability is observed. Mutations in the MSX2 and ALX4 genes have been identified for some cases. OMIM: 168500. |
| TERMUI |
T809189 T841329 T809191 T809188 T809192 T809190 T809187 |
| TH |
OMIM (2013) GHR (2014) |
| tui |
T019 |
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