NOS3

nitric oxide synthase 3
OMIM: 163729, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red NOS3 in Familial Meniere Disease

Level 3: Other hearing and ear disorders
Level 2: Hearing and ear disorders
Version 1.4

review Not set
Sources
  • Literature
Amber NOS3 in Cerebral vascular malformations


Level 2: Neurology
Version 4.10
Latest signed off version: v4.0 (30 Apr 2025)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Moyamoya disease, MONDO:0016820
Tags
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