NM_001130144.3(LTBP3):c.2889C>T (p.Ser963=) AND Brachyolmia-amelogenesis imperfecta syndrome
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 25, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000539135.9
Allele description [Variation Report for NM_001130144.3(LTBP3):c.2889C>T (p.Ser963=)]
NM_001130144.3(LTBP3):c.2889C>T (p.Ser963=)
Condition(s)
- Name:
- Brachyolmia-amelogenesis imperfecta syndrome
- Synonyms:
- Verloes Bourguignon syndrome; Skeletal dysplasia with amelogenesis imperfecta and platyspondyly; Platyspondyly with amelogenesis imperfecta; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0011018; MedGen: C1832594; Orphanet: 2899; OMIM: 601216
Assertion and evidence details
Last Updated: Feb 28, 2024