Keratosis Palmoplantaris Striata Iii; Ppks3
Clinical Features
Phenotypes and symptoms related to Keratosis Palmoplantaris Striata Iii; Ppks3
- Palmoplantar keratoderma
Incidence and onset information
— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)— No data available about the known clinical features onset.
Alternative names
Keratosis Palmoplantaris Striata Iii; Ppks3 Is also known as kpps3, keratoderma, palmoplantar, striate form iii, striate palmoplantar keratoderma iii, sppk3.
Researches and researchers
Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.Keratosis Palmoplantaris Striata Iii; Ppks3 Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
---|
![]() By Institute for Human Genetics University Clinic Freiburg (Germany).
KRT1
Specificity
100 %
Genes
100 % |
![]() By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain).
KRT1
Specificity
100 %
Genes
100 % |
![]() By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain).
KRT1
Specificity
100 %
Genes
100 % |
![]() By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain).
KRT1
Specificity
100 %
Genes
100 % |
![]() By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain).
KRT1
Specificity
100 %
Genes
100 % |
![]() By CGC Genetics (Portugal).
KRT1
Specificity
100 %
Genes
100 % |
![]() By CGC Genetics (Portugal).
DST, FERMT1, COL17A1, COL7A1, DSP, EXPH5, ITGA3, ITGA6, ITGB4, KRT1, KRT10, KRT14, KRT5, LAMA3, LAMB3, LAMC2, MMP1, PLEC
Specificity
6 %
Genes
100 % |
![]() By PreventionGenetics PreventionGenetics (United States).
SLC27A4, ST14, TGM1, ALOXE3, ABCA12, CLDN1, POMP, PNPLA1, ABHD5, LIPN, CERS3, CYP4F22, NIPAL4, ALOX12B, AP1S1, KRT1, KRT10, KRT2, KRT9
Specificity
6 %
Genes
100 % |
You can get up to 23 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
OMIM MESH Rare Disease Search EngineIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like HYPOBETALIPOPROTEINEMIA, FAMILIAL, 1; FHBL1 LEBER CONGENITAL AMAUROSIS 10; LCA10 ASPERGER SYNDROME, SUSCEPTIBILITY TO, 1; ASPG1 LANGER MESOMELIC DYSPLASIA; LMD CANAVAN DISEASE MICROCEPHALY 12, PRIMARY, AUTOSOMAL RECESSIVE; MCPH12