MEOX1

Red MEOX1 in Familial Neural Tube Defects

Version 1.10

Sources

• Radboud University Medical Center, Nijmegen

Phenotypes

• Klippel-Feil syndrome

Green MEOX1 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

• NHS GMS
• Expert Review Green
• Expert list
• Radboud University Medical Center, Nijmegen

Phenotypes

• Klippel-Feil syndrome 2 214300

Green MEOX1 in Fetal anomalies

Version 3.164
Latest signed off version: v3.0 (22 Mar 2023)

Sources

• Expert Review Green
• PAGE DD-Gene2Phenotype

Phenotypes

• Klippel-Feil syndrome 2, OMIM:214300
• Klippel-Feil syndrome 2, autosomal recessive, MONDO:0008958

Green MEOX1 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

• KLIPPEL-FEIL ANOMALY 118100

Amber MEOX1 in Clefting

Level 3: Dysmorphic disorders
Level 2: Dysmorphic and congenital abnormality syndromes
Version 4.110
Latest signed off version: v4.0 (22 Mar 2023)

Component of the following Super Panels:

Sources

• Expert Review Amber

Phenotypes

• KLIPPEL-FEIL SYNDROME 2, AUTOSOMAL RECESSIVE
• KFS2

Green MEOX1 in Severe Paediatric Disorders

Version 1.184

Sources

• Next Generation Children Project
• Expert Review Green
• Expert list

Phenotypes

• Klippel-Feil syndrome 2, 214300