CCND1

cyclin D1
OMIM: 168461, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red CCND1 in Familial Meniere Disease

Level 3: Other hearing and ear disorders
Level 2: Hearing and ear disorders
Version 1.1

review Not set
Sources
  • Literature

Red CCND1 in COVID-19 research


Level 2: Viral research
Version 1.77

review Not set
Sources
  • OMIM

Red CCND1 in Ductal plate malformation


Version 1.16

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert list
Phenotypes
  • {von Hippel-Lindau syndrome, modifier of} (193300)
  • {Colorectal cancer, susceptibility to} (114500)