Search Ontology:
Human Disease

parietal foramina

Term ID
DOID:0060285
Synonyms
  • Caitlin marks
  • enlarged parietal foramina
  • hereditary cranium bifidum
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. https://ghr.nlm.nih.gov/condition/enlarged-parietal-foramina
References
Ontology
Human Disease   ( DOID:0060285 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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