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DO Term : parietal foramina [DOID:0060285] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

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.

synonyms:
OMIM:168500,
enlarged parietal foramina,
SNOMEDCT_US_2023_03_01:718099006,
168500,
UMLS_CUI:C1868598,
OMIM:609566,
Caitlin marks,
MESH:C566826,
OMIM:609597,
ORDO:60015,
609566,
hereditary cranium bifidum,
609597

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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