MeSH Treeview
Query OMIM entry list
601492
-
HYALURONIDASE DEFICIENCY
→
High-scoring List
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Mucopolysaccharidoses
Lysosomal Storage Diseases
Mucopolysaccharidoses
Skin and Connective Tissue Diseases
Connective Tissue Diseases
Mucinoses
Mucopolysaccharidoses
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Mucopolysaccharidoses
Lysosomal Storage Diseases
Mucopolysaccharidoses
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Growth Disorders
Database Center for Life Science
