CNTN4

contactin 4
OMIM: 607280, Gene2Phenotype

2 panels

Panel	Reviews	Mode of inheritance	Details
Amber CNTN4 in Autism Version 0.36	review	Not set	Sources Expert Review Amber SFARI
Red CNTN4 in Intellectual disability Level 3: Neurodevelopmental disorders Level 2: Neurology and neurodevelopmental disorders Version 6.13 Latest signed off version: v6.0 (1 May 2024) Component of the following Super Panels: Childhood onset leukodystrophy Hypotonic infant Paediatric disorders	review	Not set	Sources Victorian Clinical Genetics Services

Panel

Reviews

Mode of inheritance

Details

Amber CNTN4 in Autism

Version 0.36

review

Not set

Sources

Expert Review Amber
SFARI

Red CNTN4 in Intellectual disability

Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 6.13
Latest signed off version: v6.0 (1 May 2024)

Component of the following Super Panels:

Childhood onset leukodystrophy

Hypotonic infant

Paediatric disorders

review

Not set

Sources

Victorian Clinical Genetics Services