MeSH term
Frequency | Condition_Probility | Bipolar Disorder/*genetics | 2 | 1.0 |
Ca(2+)-Transporting ATPase/genetics | 3 | 33.0 |
Female | 21 | 0.0 |
Genetic Markers | 2 | 0.0 |
Genetic Predisposition to Disease | 2 | 0.0 |
Humans | 32 | 0.0 |
Keratosis Follicularis/*genetics | 9 | 60.0 |
Male | 19 | 0.0 |
Pedigree | 10 | 0.0 |
Research Support, Non-U.S. Gov't | 20 | 0.0 |
Adolescent | 3 | 0.0 |
Adult | 10 | 0.0 |
Aged | 7 | 0.0 |
Child | 2 | 0.0 |
Child, Preschool | 2 | 0.0 |
DNA Mutational Analysis/methods | 2 | 0.0 |
Keratosis Follicularis/epidemiology/*genetics | 2 | 100.0 |
Middle Aged | 12 | 0.0 |
Polymerase Chain Reaction | 4 | 0.0 |
Base Sequence | 3 | 0.0 |
DNA Primers | 2 | 0.0 |
*Mutation | 6 | 0.0 |
Gene Deletion | 5 | 0.0 |
Mutation, Missense | 3 | 0.0 |
Calcium/metabolism | 2 | 0.0 |
Keratinocytes/metabolism | 2 | 1.0 |
Mutation | 4 | 0.0 |
Keratosis Follicularis/*enzymology | 2 | 100.0 |
Amino Acid Substitution | 2 | 0.0 |
Asian Continental Ancestry Group/*genetics | 2 | 0.0 |
Ca(2+)-Transporting ATPase/*genetics | 13 | 50.0 |
Molecular Sequence Data | 4 | 0.0 |
Animals | 4 | 0.0 |
Mice | 3 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 7 | 0.0 |
DNA Mutational Analysis | 6 | 0.0 |
*Chromosomes, Human, Pair 12 | 3 | 1.0 |
Genotype | 7 | 0.0 |
Linkage (Genetics) | 2 | 0.0 |
Chromosome Mapping | 3 | 0.0 |
Phenotype | 6 | 0.0 |
Isoenzymes/genetics | 2 | 0.0 |
Keratosis Follicularis/*genetics/pathology | 3 | 75.0 |
Codon, Nonsense | 3 | 2.0 |
Chromosomes, Human, Pair 12/*genetics | 2 | 1.0 |
Lod Score | 2 | 0.0 |
Keratosis Follicularis/*metabolism | 2 | 100.0 |
Amino Acid Sequence | 2 | 0.0 |
In Situ Hybridization, Fluorescence | 2 | 0.0 |
Pemphigus, Benign Familial/*genetics/pathology | 2 | 100.0 |
Membrane Proteins/genetics | 2 | 0.0 |
Haplotypes | 2 | 0.0 |
Reverse Transcriptase Polymerase Chain Reaction | 2 | 0.0 |
Skin/pathology | 3 | 1.0 |
Family Health | 3 | 0.0 |
Heterozygote | 2 | 0.0 |
