NM_018344.6(SLC29A3):c.821A>G (p.Glu274Gly) AND H syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 22, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002048297.6
Allele description [Variation Report for NM_018344.6(SLC29A3):c.821A>G (p.Glu274Gly)]
NM_018344.6(SLC29A3):c.821A>G (p.Glu274Gly)
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
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Acute kidney injury
Acute kidney injuryMedGen
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C2609414[conceptid] (1)
MedGen
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PREDICTED: Homo sapiens suppressor of cytokine signaling 6 (SOCS6), transcript variant X7, mRNAgi|2217318059|ref|XM_047437940.1|Nucleotide
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Homo sapiens erythrocyte membrane protein band 4.1 like 3 (EPB41L3), transcript ...
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Last Updated: Sep 29, 2024