MeSH term
Frequency | Condition_Probility | DNA/chemistry/genetics | 2 | 0.0 |
DNA Mutational Analysis | 7 | 0.0 |
Hearing Loss, Sensorineural/complications/*genetics | 2 | 33.0 |
Humans | 29 | 0.0 |
Mutation | 9 | 0.0 |
Myosins/*genetics | 13 | 25.0 |
Polymorphism, Single-Stranded Conformational | 2 | 0.0 |
Research Support, Non-U.S. Gov't | 24 | 0.0 |
Retinitis Pigmentosa/complications/*genetics | 3 | 37.0 |
Syndrome | 14 | 0.0 |
Base Sequence | 7 | 0.0 |
Family Health | 2 | 0.0 |
Female | 13 | 0.0 |
Genotype | 5 | 0.0 |
Male | 13 | 0.0 |
Myosins/genetics | 2 | 11.0 |
Pedigree | 10 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 11 | 0.0 |
Adult | 7 | 0.0 |
Aged | 3 | 0.0 |
Audiometry | 2 | 4.0 |
Carrier Proteins/*genetics | 2 | 0.0 |
Disease Progression | 3 | 0.0 |
Middle Aged | 5 | 0.0 |
Mutation/*genetics | 3 | 0.0 |
*Phenotype | 2 | 0.0 |
Animals | 15 | 0.0 |
Cells, Cultured | 2 | 0.0 |
Deafness/genetics | 2 | 4.0 |
Electrophysiology | 2 | 0.0 |
Mice | 12 | 0.0 |
Myosins/genetics/*physiology | 2 | 100.0 |
Adolescent | 3 | 0.0 |
Child | 4 | 0.0 |
Child, Preschool | 2 | 0.0 |
Connexins/genetics | 2 | 4.0 |
Exons/genetics | 3 | 0.0 |
Phenotype | 5 | 0.0 |
Aging | 2 | 0.0 |
Deafness/genetics/*physiopathology | 2 | 66.0 |
Mice, Inbred BALB C | 2 | 0.0 |
Mice, Inbred C57BL | 2 | 0.0 |
Mice, Inbred CBA | 3 | 0.0 |
Mice, Mutant Strains | 3 | 0.0 |
*Mutation | 8 | 0.0 |
Abnormalities, Multiple/*genetics | 2 | 0.0 |
Alternative Splicing/genetics | 2 | 1.0 |
Heterozygote Detection | 2 | 0.0 |
Amino Acid Sequence | 3 | 0.0 |
Hearing Loss, Sensorineural/*genetics | 4 | 4.0 |
Molecular Sequence Data | 4 | 0.0 |
Reverse Transcriptase Polymerase Chain Reaction | 2 | 0.0 |
Alleles | 4 | 0.0 |
Exons | 3 | 0.0 |
Heterozygote | 4 | 0.0 |
Introns | 2 | 0.0 |
Protein Structure, Tertiary | 2 | 0.0 |
Retinal Degeneration/*genetics | 2 | 5.0 |
Transcription, Genetic | 2 | 0.0 |
Genes, Recessive | 3 | 0.0 |
Chromosome Mapping | 5 | 0.0 |
Amino Acid Substitution | 2 | 0.0 |
*Gene Expression Regulation | 2 | 0.0 |
Hearing Loss, Sensorineural/*genetics/metabolism | 2 | 50.0 |
Hela Cells | 2 | 0.0 |
Mutation, Missense | 2 | 0.0 |
Pigment Epithelium of Eye/metabolism | 2 | 6.0 |
Polymerase Chain Reaction | 2 | 0.0 |
Retinitis Pigmentosa/*genetics/metabolism | 2 | 28.0 |
Vestibular Diseases/*genetics/metabolism | 2 | 100.0 |
Chromosomes, Human, Pair 11 | 3 | 0.0 |
Disease Models, Animal | 2 | 0.0 |
Retinitis Pigmentosa/*genetics | 2 | 1.0 |
Microscopy, Electron, Scanning | 3 | 1.0 |
Genes, Dominant | 2 | 0.0 |
Deafness/*genetics | 3 | 2.0 |
*Genes, Recessive | 2 | 1.0 |
Auditory Threshold | 2 | 5.0 |
Cadherins/*genetics | 2 | 2.0 |
Age of Onset | 2 | 0.0 |
