MeSH Treeview
Query OMIM entry list
602522
-
BARTTER SYNDROME, INFANTILE, WITH SENSORINEURAL DEAFNESS
→
High-scoring List
Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Base Sequence
Repetitive Sequences, Nucleic Acid
Genetic Phenomena
Consanguinity
Founder Effect
Genetic Processes
Breeding
Inbreeding
Consanguinity
Mutagenesis
Sequence Deletion
Gene Deletion
Recombination, Genetic
Genetic Structures
Base Sequence
Repetitive Sequences, Nucleic Acid
Chromosome Structures
Centromere
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 1-3
Chromosomes, Human, Pair 1
Genome
Genome Components
Genes
Gene Components
Exons
Genetic Variation
Mutation
Mutation, Missense
Point Mutation
Sequence Deletion
Gene Deletion
Polymorphism, Genetic
Polymorphism, Single-Stranded Conformational
Genotype
Haplotypes
Genetic Linkage
Phenotype
Genetic Markers
Reproductive and Urinary Physiological Phenomena
Urinary Tract Physiological Phenomena
Urinary Tract Physiological Processes
Diuresis
Database Center for Life Science
