Phenotypic Series - PS603165
Dermatitis, atopic - PS603165 - 9 Entries
| Location | Phenotype | Inheritance |
Phenotype mapping key |
Phenotype MIM number |
Gene/Locus |
Gene/Locus MIM number |
|---|---|---|---|---|---|---|
| 1q21.3 | {Dermatitis, atopic, susceptibility to, 2} | AD | 3 | 605803 | FLG | 135940 |
| 3p24 | {Dermatitis, atopic, susceptibility to, 9} | 2 | 613519 | ATOD9 | 613519 | |
| 3q21 | {Dermatitis, atopic, susceptibility to, 1} | AD | 2 | 603165 | ATOD1 | 603165 |
| 4q22.1 | {Dermatitis, atopic, susceptibility to, 8} | 2 | 613518 | ATOD8 | 613518 | |
| 5q31-q33 | {Dermatitis, atopic, susceptibility to, 6} | 2 | 605845 | ATOD6 | 605845 | |
| 11q13.5 | {Dermatitis, atopic, susceptibility to, 7} | 2 | 613064 | ATOD7 | 613064 | |
| 13q12-q14 | {Dermatitis, atopic, susceptibility to, 5} | 2 | 605844 | ATOD5 | 605844 | |
| 17q25.3 | {Dermatitis, atopic, susceptibility to, 4} | 2 | 605805 | ATOD4 | 605805 | |
| 20p | {Dermatitis, atopic, susceptibility to, 3} | 2 | 605804 | ATOD3 | 605804 |
| Phenotype Mapping Key |
|---|
| 1 - The disorder is placed on the map due to its association with a gene, but the underlying defect is not known |
| 2 - The disorder was placed on the map by statistical methods |
| 3 - The molecular basis of the disorder is known |
| 4 - A contiguous gene duplication or deletion syndrome in which multiple genes are involved |
| Inheritance Abbreviations | |
|---|---|
| ?AD | ?Autosomal dominant |
| ?XLR | ?X-linked recessive |
| AD | Autosomal dominant |
| AR | Autosomal recessive |
| PD | Pseudoautosomal dominant |
| PR | Pseudoautosomal recessive |
| DD | Digenic dominant |
| DR | Digenic recessive |
| ICB | Inherited chromosomal imbalance |
| IC | Isolated cases |
| Mi | Mitochondrial |
| Mu | Multifactorial |
| SMo | Somatic mosaicism |
| SMu | Somatic mutation |
| XL | X-linked |
| XLD | X-linked dominant |
| XLR | X-linked recessive |
| YL | Y-linked |