ANXA3

1 panel

Panel	Reviews	Mode of inheritance	Details
Red ANXA3 in Arthrogryposis Level 3: Neuromuscular disorders Level 2: Neurology and neurodevelopmental disorders Version 5.31 Latest signed off version: v5.0 (22 Mar 2023)	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Literature Phenotypes unknown equinus deformity

Panel

Reviews

Mode of inheritance

Details

Level 3: Neuromuscular disorders
Level 2: Neurology and neurodevelopmental disorders
Version 5.31
Latest signed off version: v5.0 (22 Mar 2023)

review

MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown