NM_002449.5(MSX2):c.*1006dup AND Craniosynostosis syndrome
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jun 14, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000327898.5
Allele description [Variation Report for NM_002449.5(MSX2):c.*1006dup]
NM_002449.5(MSX2):c.*1006dup
Condition(s)
- Name:
- Craniosynostosis syndrome
- Synonyms:
- Craniosynostosis
- Identifiers:
- MONDO: MONDO:0015469; MeSH: D003398; MedGen: C0010278; OMIM: PS123100; Human Phenotype Ontology: HP:0001363
Assertion and evidence details
Last Updated: Apr 9, 2023