CADM3

cell adhesion molecule 3
OMIM: 609743, Gene2Phenotype

1 panel

Panel	Reviews	Mode of inheritance	Details
Amber CADM3 in Hereditary neuropathy or pain disorder Version 3.94 Latest signed off version: v3.24 (15 May 2023)	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Literature Phenotypes Charcot-Marie-Tooth disease, axonal, type 2FF, OMIM:619519 Tags watchlist Q2_24_promote_green Q2_24_NHS_review

Panel

Reviews

Mode of inheritance

Details

Version 3.94
Latest signed off version: v3.24 (15 May 2023)

review

MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted