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Query OMIM entry list
600886
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HYPERFERRITINEMIA-CATARACT SYNDROME
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Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Base Sequence
Molecular Conformation
Nucleic Acid Conformation
Genetic Phenomena
Genetic Structures
Base Sequence
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 19-20
Chromosomes, Human, Pair 19
Genetic Code
Codon
Codon, Initiator
Genome
Genome Components
Genes
Gene Components
Codon
Codon, Initiator
Genes, Dominant
Nucleic Acid Conformation
Genetic Variation
Mutation
Point Mutation
Inheritance Patterns
Genes, Dominant
Database Center for Life Science