Erythrokeratoderma

MONDO:0019270

An umbrella term for a group of rare genetic skin disorders characterized by well-demarcated plaques of reddened, dry and thickened skin. Typically, these lesions are distributed symmetrically on the body and tend to slowly expand and progress over time.

12 clinical trials for this condition and its sub-types, 0 tagged with Erythrokeratoderma itself.

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Where it sits in the disease tree

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↑ Epidermal disease (128)

Sub-types of Erythrokeratoderma

Pityriasis rubra pilaris 2 trials · 12 incl. sub-types
3 sub-types
- Familial pityriasis rubra pilaris 10 trials
- Adult onset pityriasis rubra pilaris 0 trials
- Juvenile onset pityriasis rubra pilaris 0 trials
MEDNIK syndrome 0 trials
Cardiomyopathy, dilated, with wooly hair, keratoderma, and tooth agenesis 0 trials
Erythrokeratoderma en cocardes 0 trials
Erythrokeratodermia variabilis 0 trials
8 sub-types
- Erythrokeratodermia variabilis et progressiva 1 0 trials
- Erythrokeratodermia variabilis et progressiva 2 0 trials
- Erythrokeratodermia variabilis et progressiva 3 0 trials
- Erythrokeratodermia variabilis et progressiva 4 0 trials
- Erythrokeratodermia variabilis et progressiva 5 0 trials
- Erythrokeratodermia variabilis et progressiva 6 0 trials
- Erythrokeratodermia variabilis et progressiva 7 0 trials
- Transgrediens et progrediens palmoplantar keratoderma 0 trials
Spinocerebellar ataxia type 34 0 trials

Including sub-types (12) Tagged with Erythrokeratoderma (0)

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