FAM92A

family with sequence similarity 92 member A
OMIM: 617273, Gene2Phenotype

1 panel

Panel	Reviews	Mode of inheritance	Details
Amber FAM92A in Limb disorders Version 5.4 Latest signed off version: v5.0 (1 May 2024) Component of the following Super Panels: Paediatric disorders	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes postaxial polydactyly type A9

Panel

Reviews

Mode of inheritance

Details

Version 5.4
Latest signed off version: v5.0 (1 May 2024)

Component of the following Super Panels:

Paediatric disorders

review

BIALLELIC, autosomal or pseudoautosomal