MeSH Treeview
Query OMIM entry list
135290
-
DESMOID DISEASE, HEREDITARY
→
High-scoring List
Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Amino Acid Sequence
Base Sequence
Repetitive Sequences, Nucleic Acid
Interspersed Repetitive Sequences
Retroelements
Short Interspersed Nucleotide Elements
Alu Elements
Genetic Phenomena
Genetic Processes
Gene Expression Regulation
Mutagenesis
Sequence Deletion
Chromosome Deletion
Genetic Structures
Base Sequence
Repetitive Sequences, Nucleic Acid
Interspersed Repetitive Sequences
Retroelements
Short Interspersed Nucleotide Elements
Alu Elements
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 4-5
Chromosomes, Human, Pair 5
Genetic Code
Codon
Genome
Genome Components
DNA, Intergenic
Untranslated Regions
3' Untranslated Regions
Genes
Alleles
Gene Components
Codon
Untranslated Regions
3' Untranslated Regions
Genes, Neoplasm
Genes, Tumor Suppressor
Genes, APC
Genes, Recessive
Genes, Tumor Suppressor
Genes, APC
Interspersed Repetitive Sequences
Retroelements
Short Interspersed Nucleotide Elements
Alu Elements
Genetic Variation
Mutation
Allelic Imbalance
Loss of Heterozygosity
Chromosome Deletion
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Frameshift Mutation
Germ-Line Mutation
Mutation, Missense
Sequence Deletion
Chromosome Deletion
Genotype
Genetic Linkage
Phenotype
Ploidies
Aneuploidy
Monosomy
Chromosome Deletion
Database Center for Life Science
