MeSH Treeview
Query OMIM entry list
155900
-
MELKERSSON-ROSENTHAL SYNDROME
→
High-scoring List
Genetic Phenomena
Genetic Processes
Mutagenesis
Translocation, Genetic
Genetic Structures
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 6-12 and X
Chromosomes, Human, Pair 9
Chromosomes, Human, 21-22 and Y
Chromosomes, Human, Pair 21
Genome
Genome Components
Genes
Genes, Dominant
Genetic Variation
Mutation
Chromosome Aberrations
Translocation, Genetic
Inheritance Patterns
Genes, Dominant
Physiological Phenomena
Electrophysiological Phenomena
Electrophysiological Processes
Neural Conduction
Physiological Processes
Electrophysiological Processes
Neural Conduction
Musculoskeletal and Neural Physiological Phenomena
Nervous System Physiological Phenomena
Nervous System Physiological Processes
Neural Conduction
Database Center for Life Science
