TNNT3

troponin T3, fast skeletal type
OMIM: 600692
PanelMode of inheritanceDetails
3 panels
R-numbers: R83
Signed-off version 4.1
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Arthrogryposis, distal, type 2B2, OMIM:618435, Arthrogryposis, distal, type 2B2, MONDO:0032750
Component of the following Super Panels:
  • - Hypotonic infant
  • - Neuromuscular disorders
R-numbers: R81
Signed-off version 3.1
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Arthrogryposis, distal, type 2B2, OMIM:618435, Arthrogryposis, distal, type 2B2, MONDO:0032750
R-numbers: R21, R412
Signed-off version 2.1
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Arthrogryposis, distal, type 2B2, OMIM:618435, Arthrogryposis, distal, type 2B2, MONDO:0032750