IL11

interleukin 11
OMIM: 147681, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red IL11 in Familial Hirschsprung Disease

Level 3: Gastrointestinal disorders
Level 2: Gastroenterological disorders
Version 1.10

review Unknown
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • risk of HSCR
Red IL11 in DDG2P


Version 4.3
Latest signed off version: v4.0 (1 May 2024)

Component of the following Super Panels:

  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • DD-Gene2Phenotype
    • Expert Review Red
    Phenotypes
    • CRANIOSYNOSTOSIS AND DENTAL ANOMALIES 614188