EPHA7

EPH receptor A7
OMIM: 602190, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber EPHA7 in Mendeliome


Version 1.1891

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Expert Review
Phenotypes
  • Neurodevelopmental disorder MONDO:0700092,EPHA7-related
Tags
  • SV/CNV

Amber EPHA7 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 0.6063

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Neurodevelopmental disorder MONDO:0700092,EPHA7-related
Tags
  • SV/CNV