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Query OMIM entry list
104200
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ALPORT SYNDROME, AUTOSOMAL DOMINANT
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Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Amino Acid Sequence
Base Sequence
Genetic Phenomena
Consanguinity
Genetic Processes
Breeding
Inbreeding
Consanguinity
Heredity
Mutagenesis
Sequence Deletion
Gene Deletion
Genetic Structures
Base Sequence
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 6-12 and X
Chromosomes, Human, Pair 11
Sex Chromosomes
X Chromosome
Genome
Genome Components
Genes
Gene Components
Exons
Genes, Dominant
Genes, Recessive
Genetic Variation
Mutation
Point Mutation
Sequence Deletion
Gene Deletion
Polymorphism, Genetic
Polymorphism, Single-Stranded Conformational
Genotype
Heterozygote
Homozygote
Inheritance Patterns
Genes, Dominant
Genes, Recessive
Genetic Linkage
Lod Score
Phenotype
Genetic Markers
Physiological Phenomena
Physiological Processes
Homeostasis
Reproductive and Urinary Physiological Phenomena
Reproductive Physiological Phenomena
Sex
Musculoskeletal and Neural Physiological Phenomena
Nervous System Physiological Phenomena
Nervous System Physiological Processes
Sensation
Hearing
Immune System Phenomena
Immune System Processes
Transplantation Immunology
Host vs Graft Reaction
Graft Rejection
Database Center for Life Science
