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Query OMIM entry list
601471
HCFP1
FACIAL PARESIS, HEREDITARY, CONGENITAL
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Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Amino Acid Sequence
Base Sequence
Sequence Homology
Sequence Homology, Amino Acid
Cell Physiological Phenomena
Cell Count
Genetic Phenomena
Genetic Processes
Gene Expression Regulation
Gene Expression Regulation, Developmental
Genetic Structures
Base Sequence
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 1-3
Chromosomes, Human, Pair 3
Genome
Genome Components
Genes
Genes, Dominant
Genetic Variation
Genetic Heterogeneity
Genotype
Genetic Predisposition to Disease
Haplotypes
Heterozygote
Inheritance Patterns
Genes, Dominant
Genetic Linkage
Phenotype
Genetic Markers
Sequence Homology
Sequence Homology, Amino Acid
Physiological Phenomena
Physiological Processes
Growth and Development
Morphogenesis
Embryonic and Fetal Development
Embryonic Development
Reproductive and Urinary Physiological Phenomena
Reproductive Physiological Phenomena
Reproductive Physiological Processes
Reproduction
Embryonic and Fetal Development
Embryonic Development
Circulatory and Respiratory Physiological Phenomena
Cardiovascular Physiological Phenomena
Cardiovascular Physiological Processes
Neovascularization, Physiologic
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