NM_001002295.2(GATA3):c.1179C>T (p.Asn393=) AND Hypoparathyroidism, deafness, renal disease syndrome
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000395824.6
Allele description [Variation Report for NM_001002295.2(GATA3):c.1179C>T (p.Asn393=)]
NM_001002295.2(GATA3):c.1179C>T (p.Asn393=)
Condition(s)
- Name:
- Hypoparathyroidism, deafness, renal disease syndrome (HDRS)
- Synonyms:
- Barakat syndrome; Hypoparathyroidism, sensorineural deafness, and renal dysplasia; HDR syndrome; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0007797; MedGen: C1840333; Orphanet: 2237; OMIM: 146255
Assertion and evidence details
Last Updated: Apr 15, 2024