1. Genes and Genomic Entities
  2. CALCRL

CALCRL

calcitonin receptor like receptor
OMIM: 114190, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red CALCRL in Fetal anomalies


Version 4.1
Latest signed off version: v4.0 (1 May 2024)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Lymphatic malformation 8, OMIM:618773
  • Lymphatic malformation 8, MONDO:0032907
  • Hydrops fetalis