MeSH term
Frequency | Condition_Probility | Amino Acid Sequence | 2 | 0.0 |
Base Sequence | 2 | 0.0 |
Chromosome Mapping | 6 | 0.0 |
*Chromosomes, Human, Pair 10 | 5 | 2.0 |
Foot Deformities, Congenital/*genetics | 6 | 46.0 |
Hand Deformities, Congenital/*genetics | 7 | 43.0 |
Humans | 12 | 0.0 |
Molecular Sequence Data | 2 | 0.0 |
Mutation | 2 | 0.0 |
Research Support, Non-U.S. Gov't | 8 | 0.0 |
*Chromosome Aberrations | 2 | 0.0 |
Chromosomes, Human, Pair 10/genetics | 2 | 2.0 |
Pedigree | 6 | 0.0 |
Polymorphism, Single-Stranded Conformational | 2 | 0.0 |
Chromosomes, Human, Pair 10/*genetics | 3 | 2.0 |
Linkage (Genetics) | 5 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 6 | 0.0 |
Female | 7 | 0.0 |
Lod Score | 2 | 0.0 |
Male | 5 | 0.0 |
Phenotype | 4 | 0.0 |
Infant, Newborn | 2 | 0.0 |
Abnormalities, Multiple/*genetics | 3 | 0.0 |
Abnormalities, Multiple/*genetics/pathology | 2 | 2.0 |
Fingers/abnormalities | 2 | 13.0 |
Foot Deformities/*genetics | 2 | 66.0 |
Hand Deformities/*genetics | 2 | 50.0 |
Proteins/*genetics | 2 | 0.0 |