NM_000529.2(MC2R):c.666C>G (p.Thr222=) AND Glucocorticoid deficiency 1
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 15, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001127291.4
Allele description [Variation Report for NM_000529.2(MC2R):c.666C>G (p.Thr222=)]
NM_000529.2(MC2R):c.666C>G (p.Thr222=)
Condition(s)
- Name:
- Glucocorticoid deficiency 1 (GCCD1)
- Synonyms:
- FAMILIAL GLUCOCORTICOID DEFICIENCY 1; ACTH resistance; Adrenal unresponsiveness to acth; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0024536; MedGen: C4049650; Orphanet: 361; OMIM: 202200
Assertion and evidence details
Last Updated: Apr 9, 2023