KIRREL3

kirre like nephrin family adhesion molecule 3
OMIM: 607761, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red KIRREL3 in Mendeliome


Version 2.629

3 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Expert list
Phenotypes
  • complex neurodevelopmental disorder, MONDO:0100038, KIRREL3-related
Tags
  • disputed

Red KIRREL3 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 2.159

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Genetic Health Queensland
Phenotypes
  • complex neurodevelopmental disorder, MONDO:0100038, KIRREL3-related
Tags
  • disputed