MeSH Treeview
Query OMIM entry list
239510
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HYPERPROLINEMIA, TYPE II
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Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Amino Acid Sequence
Base Sequence
Sequence Homology
Sequence Homology, Amino Acid
Genetic Phenomena
Consanguinity
Genetic Processes
Biological Evolution
Evolution, Molecular
Breeding
Inbreeding
Consanguinity
Gene Expression
Mutagenesis
Sequence Deletion
Chromosome Deletion
Genetic Structures
Base Sequence
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 21-22 and Y
Chromosomes, Human, Pair 22
Genome
Genome Components
Genes
Alleles
Genetic Variation
Mutation
Allelic Imbalance
Loss of Heterozygosity
Chromosome Deletion
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Frameshift Mutation
Point Mutation
Sequence Deletion
Chromosome Deletion
Polymorphism, Genetic
Genotype
Heterozygote
Homozygote
Phenotype
Ploidies
Aneuploidy
Monosomy
Chromosome Deletion
Sequence Homology
Sequence Homology, Amino Acid
Biological Phenomena
Biological Processes
Biological Evolution
Evolution, Molecular
Database Center for Life Science
