CLDN11

claudin 11
OMIM: 601326, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Green CLDN11 in Mendeliome


Version 2.0

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Hypomyelinating leukodystrophy-22, MIM#619328

Green CLDN11 in Leukodystrophy


Level 2: Neurology and neurodevelopmental disorders
Version 1.0

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Hypomyelinating leukodystrophy-22, MIM#619328