MAOB

monoamine oxidase B
OMIM: 309860, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red MAOB in Cerebral Palsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.389

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Cerebral palsy

Red MAOB in Mendeliome


Version 1.2302

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Expert Review
Phenotypes
  • Cerebral palsy