Psoriasis 2; Psors2

Table of contents:

Description
Related genes
Clinical Features
Incidence and onset information
Alternative Names
Researches and researchers
Gene Panels
Sources and references

Genes related to Psoriasis 2; Psors2

CARD14

View recommended genes panels

Clinical Features

Top most frequent phenotypes and symptoms related to Psoriasis 2; Psors2

Fever
Hyperkeratosis
Arthralgia
Arthritis
Ichthyosis
Epidermal acanthosis
Inflammatory abnormality of the skin
Dermal atrophy
Scaling skin
Psoriasiform dermatitis

And another 5 symptoms. If you need more information about this disease we can help you.

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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.

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.

Psoriasis 2; Psors2 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
CARD14. By Institute for Human Genetics University Clinic Freiburg (Germany). CARD14 Specificity 100 % Genes 100 %
Psoriasis susceptibility 2 (sequence analysis of CARD14 gene). By CGC Genetics (Portugal). CARD14 Specificity 100 % Genes 100 %
Familial Pityriasis Rubra Pilaris (PRP) via CARD14 Gene Sequencing with CNV Detection. By PreventionGenetics PreventionGenetics (United States). CARD14 Specificity 100 % Genes 100 %
Periodic Fever Syndromes Sequencing Panel with CNV Detection. By PreventionGenetics PreventionGenetics (United States). TNFAIP3, TNFRSF1A, LPIN2, IL36RN, NLRP3, CARD14, NLRP12, ELANE, NOD2, MEFV, MVK, PSMB8, PSTPIP1 Specificity 8 % Genes 100 %
Pityriasis rubra pilaris. By Centogene AG - the Rare Disease Company (Germany). CARD14 Specificity 100 % Genes 100 %
Psoriasis type 2. By Centogene AG - the Rare Disease Company (Germany). CARD14 Specificity 100 % Genes 100 %
Ichthyoses and related disorders of cornification Panel. By CeGaT GmbH (Germany). SLC27A4, SNAP29, ST14, STS, TAT, TGM1, TGM5, VPS33B, ATP2C1, NSDHL, ALOXE3, WNT10A, SERPINB7, ELOVL4, ABCA12, MBTPS2, SPINK5, CARD14, CDSN, TRPV3 , (...) View the complete list with 44 more genes Panel complete gene list SLC27A4, SNAP29, ST14, STS, TAT, TGM1, TGM5, VPS33B, ATP2C1, NSDHL, ALOXE3, WNT10A, SERPINB7, ELOVL4, ABCA12, MBTPS2, SPINK5, CARD14, CDSN, TRPV3, SLURP1, CLDN1, POMP, SUMF1, KRT6C, RHBDF2, GTF2H5, PNPLA1, ABHD5, LIPN, CERS3, CSTA, CTSC, AAGAB, CYP4F22, NIPAL4, DSG1, DSP, EBP, ENPP1, ERCC2, ERCC3, FLG, ALDH3A2, ALMS1, GJB2, GJB4, GJB6, ALOX12B, AP1S1, JUP, AQP5, KRT1, KRT10, KRT14, KRT16, KRT17, KRT2, KRT6A, KRT6B, KRT9, LOR, ATP2A2, PHYH Specificity 2 % Genes 100 %
Autoinflammatory diseases Panel. By CeGaT GmbH (Germany). SH3BP2, TNFRSF1A, LPIN2, IL36RN, RBCK1, NLRP3, CARD14, NLRP12, SLC29A3, HFE, NOD2, IL10, IL10RA, IL10RB, IL1RN, MEFV, MVK, PLCG2, PSMB8, PSTPIP1 Specificity 5 % Genes 100 %

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Sources and references

You can check the following sources for additional information.

OMIM Rare Disease Symptoms Checker

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