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DO Term : craniosynostosis 2 [DOID:0061009] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A craniosynostosis characterized by a highly variable craniosynostosis with frontal bossing, turribrachycephaly and cloverleaf skull anomaly that has_material_basis_in heterozygous mutation in the MSX2 gene on chromosome 5q35.
  • synonyms:
  • 604757,
  • GARD:5538,
  • ORDO:1541,
  • OMIM:604757,
  • Warman-Mulliken-Hayward syndrome,
  • Craniosynostosis Boston type,
  • Craniosynostosis Warman type,
  • CRS2
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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