| Human Disease |
Term: Keratoderma, Palmoplantar, Punctate Type IA; PPKP1A
OMIM ID: 148600
|
| Synonyms |
Keratoderma, Palmoplantar, Punctate Type I; PPKP1; Keratodermia Palmoplantaris Papulosa, Buschke-Fischer-Brauer Type; Keratosis Palmoplantaris Papulosa; Kppp1 |
| Associated Genes |
Orthologous mouse and human markers where mutations in one or both species have been associated with phenotypes characteristic of this disease.
Mouse Gene |
Human Gene |
|
Characteristics of this human disease are associated with mutations in... |
| |
|
|
|
|
 ...the human gene.
MGI data currently do not associate this disease with mutations in the orthologous mouse gene. |
| |
|
|
|
Analysis Tools