NM_018344.6(SLC29A3):c.529G>A (p.Gly177Ser) AND H syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 30, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001341013.5
Allele description [Variation Report for NM_018344.6(SLC29A3):c.529G>A (p.Gly177Ser)]
NM_018344.6(SLC29A3):c.529G>A (p.Gly177Ser)
Condition(s)
- Name:
- H syndrome
- Synonyms:
- Histiocytosis with joint contractures and sensorineural deafness; Faisalabad histiocytosis; HISTIOCYTOSIS AND LYMPHADENOPATHY WITH OR WITHOUT CUTANEOUS, CARDIAC, AND/OR ENDOCRINE FEATURES, JOINT CONTRACTURES, AND/OR DEAFNESS; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0011273; MedGen: C1864445; Orphanet: 168569; OMIM: 602782
Assertion and evidence details
Last Updated: May 7, 2024