MeSH Treeview
Query OMIM entry list
600110
STGD3
STARGARDT DISEASE 3
→
High-scoring List
Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Amino Acid Sequence
Base Sequence
Metabolic Phenomena
Pharmacokinetics
Tissue Distribution
Cell Physiological Phenomena
Cell Physiological Processes
Cell Death
Apoptosis
Cell Survival
Genetic Phenomena
Founder Effect
Genetic Processes
Mutagenesis
Sequence Deletion
Recombination, Genetic
Transfection
Genetic Structures
Base Sequence
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 6-12 and X
Chromosomes, Human, Pair 6
Chromosomes, Human, Pair 11
Chromosomes, Human, 13-15
Chromosomes, Human, Pair 13
Genetic Code
Codon
Codon, Terminator
Reading Frames
Open Reading Frames
Genome
Genome Components
DNA, Intergenic
Introns
Genes
Gene Components
Codon
Codon, Terminator
Exons
Introns
Open Reading Frames
Genes, Dominant
Genes, Recessive
Genetic Variation
Genetic Heterogeneity
Mutation
Mutation, Missense
Sequence Deletion
Polymorphism, Genetic
Polymorphism, Single-Stranded Conformational
Genotype
Haplotypes
Inheritance Patterns
Genes, Dominant
Genes, Recessive
Penetrance
Genetic Linkage
Lod Score
Phenotype
Genetic Markers
Penetrance
Physiological Phenomena
Pharmacological Phenomena
Pharmacokinetics
Tissue Distribution
Ocular Physiological Phenomena
Visual Acuity
Visual Fields
Database Center for Life Science