LRRC7

leucine rich repeat containing 7
OMIM: 614453, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Green LRRC7 in Intellectual disability


Level 2: Developmental disorders
Version 9.370
Latest signed off version: v9.0 (30 Apr 2025)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • NHS GMS
    • Literature
    • Expert Review
    Phenotypes
    • Intellectual developmental disorder, autosomal dominant 77, OMIM:621415
    • intellectual developmental disorder, autosomal dominant 77, MONDO:0980748