NM_000101.4(CYBA):c.198G>A (p.Glu66=) AND Granulomatous disease, chronic, autosomal recessive, cytochrome b-negative
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 19, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001456749.6
Allele description [Variation Report for NM_000101.4(CYBA):c.198G>A (p.Glu66=)]
NM_000101.4(CYBA):c.198G>A (p.Glu66=)
Condition(s)
- Name:
- Granulomatous disease, chronic, autosomal recessive, cytochrome b-negative
- Synonyms:
- CGD DUE TO DEFICIENCY OF THE ALPHA SUBUNIT OF CYTOCHROME b; CGD, AUTOSOMAL RECESSIVE CYTOCHROME b-NEGATIVE; CYBA DEFICIENCY; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0009308; MedGen: C1856255; Orphanet: 379; OMIM: 233690
-
Anatomy, Lymphatic System - StatPearls
Anatomy, Lymphatic System - StatPearls
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See more...Assertion and evidence details
Last Updated: Mar 5, 2024