Inherited non-medullary thyroid cancer

Gene: SDHD

Red List (low evidence)

SDHD (succinate dehydrogenase complex subunit D)
EnsemblGeneIds (GRCh38): ENSG00000204370
EnsemblGeneIds (GRCh37): ENSG00000204370
OMIM: 602690, Gene2Phenotype
SDHD is in 25 panels

1 review

Sarah Leigh (Genomics England Curator)

Red List (low evidence)

Associated with phenotype in OMIM, not in G2P. One variant reported in two unrealated cases with Cowden syndrome 3 and papillary thyroid cancer (PMID 18678321)
Created: 7 Aug 2017, 1:47 p.m.

Mode of inheritance
Unknown

Phenotypes
Cowden syndrome 3 615106

Publications

History Filter Activity

7 Aug 2017, Gel status: 0

panel promoted to version 1

Sarah Leigh (Genomics England Curator)

All genes have been reviewed and the reviews evaluated. 07.08.2017

7 Aug 2017, Gel status: 0

Created

Sarah Leigh (Genomics England Curator)

SDHD was created by sleigh

7 Aug 2017, Gel status: 0

Added New Source

Sarah Leigh (Genomics England Curator)

SDHD was added to Inherited non-medullary thyroid cancerpanel. Sources: Literature