Description
This panel was developed and is maintained by the KidGen Collaborative. It is also a consensus panel used by VCGS.

2 reviewers

  • Chirag Patel (Genetic Health Queensland)

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

5 Entities

5 reviewed, 5 green

List Entity Reviews Mode of inheritance Details
5 Entitiess
Green Green List (high evidence)
APOA1
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Amyloidosis, 3 or more types, MIM#105200
Tags
Green Green List (high evidence)
FGA
2 reviews
2 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Amyloidosis, familial visceral, MIM#105200
Tags
Green Green List (high evidence)
GSN
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Amyloidosis, Finnish type, MIM#105200
Tags
Green Green List (high evidence)
LYZ
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Amyloidosis, renal, MIM#105200
Tags
Green Green List (high evidence)
NLRP3
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Muckle-Wells syndrome, MIM#191900
Tags

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