HYAL2

hyaluronoglucosaminidase 2
OMIM: 603551, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green HYAL2 in Congenital Heart Defect


Level 2: Cardiovascular disorders
Version 0.430

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Muggenthaler-Chowdhury-Chioza syndrome, MIM# 621063

Green HYAL2 in Mendeliome


Version 1.2374

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Muggenthaler-Chowdhury-Chioza syndrome, MIM# 621063

Green HYAL2 in Clefting disorders

Level 3: Dysmorphic disorders
Level 2: Dysmorphic and congenital abnormality syndromes
Version 0.260

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert list
Phenotypes
  • Muggenthaler-Chowdhury-Chioza syndrome, MIM# 621063

Green HYAL2 in Fetal anomalies


Version 1.314

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Muggenthaler-Chowdhury-Chioza syndrome, MIM# 621063