ADGRL2

adhesion G protein-coupled receptor L2
OMIM: 607018, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red ADGRL2 in Mendeliome


Version 2.109

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Neurodevelopmental disorder, MONDO:0700092, ADGRL2-related

Red ADGRL2 in Microcephaly


Level 2: Dysmorphic and congenital abnormality syndromes
Version 2.3

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
  • Literature
Phenotypes
  • Neurodevelopmental disorder, MONDO:0700092, ADGRL2-related

Red ADGRL2 in Fetal anomalies


Version 2.3

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
  • Literature
Phenotypes
  • Neurodevelopmental disorder, MONDO:0700092, ADGRL2-related