CALCRL

calcitonin receptor like receptor
OMIM: 114190, Gene2Phenotype

1 panel

Panel	Reviews	Mode of inheritance	Details
Red CALCRL in Fetal anomalies Version 3.155 Latest signed off version: v3.0 (22 Mar 2023)	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes Lymphatic malformation 8, OMIM:618773 Lymphatic malformation 8, MONDO:0032907 Hydrops fetalis

Panel

Reviews

Mode of inheritance

Details

Version 3.155
Latest signed off version: v3.0 (22 Mar 2023)

review

BIALLELIC, autosomal or pseudoautosomal