MeSH Treeview
Query OMIM entry list
179030
PPA1
PYROPHOSPHATASE, INORGANIC, 1
→
High-scoring List
Musculoskeletal Diseases
Muscular Diseases
Mitochondrial Myopathies
Nervous System Diseases
Neuromuscular Diseases
Muscular Diseases
Mitochondrial Myopathies
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Nutritional and Metabolic Diseases
Metabolic Diseases
Mitochondrial Diseases
Mitochondrial Myopathies
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Trisomy
Chromosome Duplication
Trisomy
Translocation, Genetic
Disease
Syndrome
Database Center for Life Science
