FBXW11

Amber FBXW11 in Limb disorders

Version 4.21
Latest signed off version: v4.0 (22 Mar 2023)

Component of the following Super Panels:

Sources

• Expert Review Amber
• Literature

Phenotypes

• Neurodevelopmental, jaw, eye, and digital syndrome, OMIM:618914
• neurodevelopmental, jaw, eye, and digital syndrome, MONDO:0030057

Tags

• Q4_21_NHS_review
• Q4_23_promote_green

Amber FBXW11 in Skeletal dysplasia

Level 3: Skeletal dysplasias
Level 2: Skeletal disorders
Version 4.63
Latest signed off version: v4.0 (22 Mar 2023)

Component of the following Super Panels:

Sources

• Expert Review Amber
• Literature

Phenotypes

• Neurodevelopmental, jaw, eye, and digital syndrome, OMIM:618914
• neurodevelopmental, jaw, eye, and digital syndrome, MONDO:0030057

Tags

• Q4_23_promote_green
• Q4_23_NHS_review

Green FBXW11 in DDG2P

Version 3.88
Latest signed off version: v3.1 (22 Mar 2023)

Component of the following Super Panels:

Sources

• Expert Review Green
• DD-Gene2Phenotype

Phenotypes

• SYNDROMIC INTELLECTUAL DISABILITY 612100

Green FBXW11 in Intellectual disability - microarray and sequencing

Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 5.544
Latest signed off version: v5.0 (22 Mar 2023)

Component of the following Super Panels:

Sources

• Expert Review Green
• Literature

Phenotypes

• Neurodevelopmental, jaw, eye, and digital syndrome, OMIM:618914
• neurodevelopmental, jaw, eye, and digital syndrome, MONDO:003005