NM_001375808.2(LPIN2):c.2657C>T (p.Pro886Leu) AND Majeed syndrome
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Jul 6, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000300063.12
Allele description [Variation Report for NM_001375808.2(LPIN2):c.2657C>T (p.Pro886Leu)]
NM_001375808.2(LPIN2):c.2657C>T (p.Pro886Leu)
Condition(s)
- Name:
- Majeed syndrome (MJDS)
- Synonyms:
- Chronic recurrent multifocal osteomyelitis, congenital; Dyserythropoietic anemia, and neutrophilic dermatosis; Congenital dyserythropoietic anemia and chronic recurrent multifocal osteomyelitis; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0012316; MedGen: C1864997; Orphanet: 77297; OMIM: 609628
Assertion and evidence details
Last Updated: Dec 24, 2023