UBB

ubiquitin B
OMIM: 191339, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red UBB in Clefting

Level 3: Dysmorphic disorders
Level 2: Dysmorphic and congenital abnormality syndromes
Version 5.3
Latest signed off version: v5.0 (1 May 2024)

Component of the following Super Panels:

  • Paediatric disorders
  • review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    Phenotypes
    • Cleft palate, isolated, 119540