PanelApp (test)
  1. Genes and Genomic Entities
  2. DENND5B

DENND5B

DENN domain containing 5B
OMIM: 617279, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green DENND5B in Mendeliome


Version 1.1902

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Other
Phenotypes
  • Neurodevelopmental disorder with white matter anomalies, MONDO:0700092, DENND5B-related

Green DENND5B 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 Green
  • Other
Phenotypes
  • Neurodevelopmental disorder with white matter anomalies, MONDO:0700092, DENND5B-related

Green DENND5B in Leukodystrophy - paediatric


Level 2: Neurology and neurodevelopmental disorders
Version 0.308

Component of the following Super Panels:

  • Leukodystrophy_Superpanel
  • Progressive Neurological Conditions

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Other
    Phenotypes
    • Neurodevelopmental disorder with white matter anomalies, MONDO:0700092, DENND5B-related