OBO ID: DOID:0060285
Term Name: parietal foramina Search Ontology:
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 parietal foramina PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
ALX4 Parietal foramina 2 609597
MSX2 Parietal foramina 1 168500
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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