CNP

Panel	Reviews	Mode of inheritance	Details
Amber CNP in Mendeliome Version 1.1891	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Leukodystrophy, hypomyelinating, 20, MIM# 619071
Amber CNP in Leukodystrophy - paediatric Level 2: Neurology and neurodevelopmental disorders Version 0.308 Component of the following Super Panels: Leukodystrophy_Superpanel Progressive Neurological Conditions	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Leukodystrophy, hypomyelinating, 20, MIM# 619071

Panel

Reviews

Mode of inheritance

Details

Version 1.1891

review

BIALLELIC, autosomal or pseudoautosomal

Level 2: Neurology and neurodevelopmental disorders
Version 0.308

Component of the following Super Panels:

Leukodystrophy_Superpanel

Progressive Neurological Conditions

review

BIALLELIC, autosomal or pseudoautosomal

2 panels