MeSH Treeview
Query OMIM entry list
234100
HSS
HALLERMANN-STREIFF SYNDROME
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Genetic Phenomena
Consanguinity
Genetic Processes
Breeding
Inbreeding
Consanguinity
DNA Damage
DNA Breaks
Chromosome Breakage
Genetic Structures
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 6-12 and X
Chromosomes, Human, X
Sex Chromosomes
X Chromosome
Chromosomes, Human, X
Genetic Code
Codon
Genome
Genome Components
Genes
Gene Components
Codon
Genes, Dominant
Genetic Variation
Mutation
Chromosome Aberrations
Chromosome Breakage
Point Mutation
Genotype
Homozygote
Inheritance Patterns
Genes, Dominant
Phenotype
Reproductive and Urinary Physiological Phenomena
Reproductive Physiological Phenomena
Reproductive Physiological Processes
Reproduction
Pregnancy
Circulatory and Respiratory Physiological Phenomena
Respiratory Physiological Phenomena
Lung Compliance
Musculoskeletal and Neural Physiological Phenomena
Musculoskeletal Physiological Phenomena
Bone Density
Ocular Physiological Phenomena
Visual Acuity
Database Center for Life Science
