MeSH Treeview
Query OMIM entry list
170250
LAP3
LEUCINE AMINOPEPTIDASE 3
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Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Chromosome Disorders
Genetic Diseases, Inborn
Chromosome Disorders
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Disease
Syndrome
Database Center for Life Science
