FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term parietal foramina ID (Ontology) DOID:0060285 (Human Disease)
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.
Also Known As "Caitlin marks" ; "enlarged parietal foramina" ; "hereditary cranium bifidum"
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 Genes
 parietal foramina       3
 for disease ribbon | parietal foramina       3
 model of | parietal foramina       3
Spanning Tree (Parents/Children)
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  physical disorder
   |__neural tube defect
       |__parietal foramina  3 rec.
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Is a neural tube defect
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Synonyms
  • "Caitlin marks" EXACT
    "enlarged parietal foramina" EXACT
    "hereditary cranium bifidum" EXACT
Secondary IDs
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MESH:C566826
MIM:168500
MIM:609566
MIM:609597
ORDO:60015
SNOMEDCT_US_2023_03_01:718099006
UMLS_CUI:C1868598