MeSH Treeview
Query OMIM entry list
600273
PKDTS
POLYCYSTIC KIDNEY DISEASE, INFANTILE SEVERE, WITH TUBEROUS SCLEROSIS
→
High-scoring List
Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Base Sequence
Genetic Phenomena
Genetic Processes
Mutagenesis
Sequence Deletion
Gene Deletion
Genetic Structures
Base Sequence
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 16-18
Chromosomes, Human, Pair 16
Genetic Variation
Mutation
Sequence Deletion
Gene Deletion
Database Center for Life Science