MeSH Treeview
Query OMIM entry list
107970
ARVD1
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 1
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Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Amino Acid Sequence
Base Sequence
Sequence Homology
Sequence Homology, Amino Acid
Cell Physiological Phenomena
Cell Physiological Processes
Cell Death
Apoptosis
Genetic Phenomena
Genetic Processes
DNA Damage
Mutagenesis
Sequence Deletion
Genetic Structures
Base Sequence
Chromosome Structures
Nucleolus Organizer Region
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 1-3
Chromosomes, Human, Pair 1
Chromosomes, Human, 13-15
Chromosomes, Human, Pair 14
Genetic Code
Codon
Codon, Terminator
Codon, Nonsense
Genome
Genome Components
DNA, Intergenic
Untranslated Regions
3' Untranslated Regions
5' Untranslated Regions
Genes
Gene Components
Exons
Untranslated Regions
3' Untranslated Regions
5' Untranslated Regions
Genes, Dominant
Genetic Loci
Nucleolus Organizer Region
Genetic Variation
Mutation
Codon, Nonsense
Frameshift Mutation
Mutation, Missense
Point Mutation
Sequence Deletion
Polymorphism, Genetic
Polymorphism, Single-Stranded Conformational
Genotype
Genetic Predisposition to Disease
Inheritance Patterns
Genes, Dominant
Genetic Linkage
Lod Score
Phenotype
Genetic Markers
Sequence Homology
Sequence Homology, Amino Acid
Circulatory and Respiratory Physiological Phenomena
Cardiovascular Physiological Phenomena
Cardiovascular Physiological Processes
Hemodynamics
Myocardial Contraction
Ventricular Function
Ventricular Function, Right
Hemodynamics
Musculoskeletal and Neural Physiological Phenomena
Musculoskeletal Physiological Phenomena
Musculoskeletal Physiological Processes
Muscle Contraction
Myocardial Contraction
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