CALCRL

calcitonin receptor like receptor
OMIM: 114190, Gene2Phenotype

1 panel

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


Level 2: Fetal (including NIPD)
Version 6.140
Latest signed off version: v6.0 (30 Apr 2025)

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