Description
With thanks to Genomics England PanelApp for the original design of this panel.

3 reviewers

  • Anna Le Fevre (Victorian Clinical Genetics Services)

  • Paul De Fazio (Victorian Clinical Genetics Services)

  • Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

8 Entities

8 reviewed, 7 green

List Entity Reviews Mode of inheritance Details
8 Entitiess
Green Green List (high evidence)
ALB
2 reviews
2 green
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Green
  • Genomics England PanelApp
Phenotypes
  • Familial dysalbuminaemic hyperthyroxinaemia
  • [Dysalbuminemic hyperthyroxinemia], 615999
Tags
Green Green List (high evidence)
SECISBP2
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Genomics England PanelApp
Phenotypes
  • Thyroid hormone metabolism, abnormal, MIM# 609698
Tags
Green Green List (high evidence)
SLC16A2
1 review
1 green
X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Green
  • Genomics England PanelApp
Phenotypes
  • Allan-Herndon-Dudley syndrome, MIM# 300523
Tags
Green Green List (high evidence)
THRA
2 reviews
1 green
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Green
  • Genomics England PanelApp
Phenotypes
  • Hypothyroidism, congenital, nongoitrous, 6 614450
Tags
Green Green List (high evidence)
THRB
1 review
1 green
BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Genomics England PanelApp
Phenotypes
  • Thyroid hormone resistance, MIM# 188570
  • Thyroid hormone resistance, autosomal recessive, MIM# 274300
  • Thyroid hormone resistance, selective pituitary, MIM# 145650
Tags
Green Green List (high evidence)
TSHR
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Genomics England PanelApp
Phenotypes
  • Hyperthyroidism, nonautoimmune, MIM# 609152
Tags
Green Green List (high evidence)
TTR
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Green
  • Genomics England PanelApp
Phenotypes
  • DTTRH
  • [Dystransthyretinemic hyperthyroxinemia], 145680
Tags
Amber Amber List (moderate evidence)
TRU-TCA1-1
1 review
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Inherited thyroid metabolism disease, MONDO:0045046, TRU-TCA1-1 related
Tags

Downloads

Download lists

Download Version