FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term craniosynostosis 2 ID (Ontology) DOID:0061009 (Human Disease)
Definition 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.
Also Known As "Craniosynostosis Boston type" ; "Craniosynostosis Warman type" ; "CRS2" (for all, see Synonyms field below)
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 Genes
 craniosynostosis 2       2
 for disease ribbon | craniosynostosis 2       2
 model of | craniosynostosis 2       2
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease__
synostosis                      |
 |__craniosynostosis____________|
                                craniosynostosis 2  2 rec.
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Is a autosomal dominant disease
craniosynostosis
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Synonyms
  • "Craniosynostosis Boston type" EXACT
    "Craniosynostosis Warman type" EXACT
    "CRS2" EXACT OMO:0003012
    "Warman-Mulliken-Hayward syndrome" EXACT
Secondary IDs
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GARD:5538
MIM:604757
ORDO:1541