CALCRL

calcitonin receptor like receptor
OMIM: 114190, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red CALCRL in Hydrops fetalis


Level 2: Dysmorphic and congenital abnormality syndromes
Version 0.313

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Lymphatic malformation 8 (MIM# 618773)
  • hydrops fetalis

Red CALCRL in Mendeliome


Version 1.1891

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • ?Lymphatic malformation 8 (MIM# 618773)
  • hydrops fetalis

Red CALCRL in Fetal anomalies


Version 1.255

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