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Dictionary » Erythrokeratodermia ataxia

Erythrokeratodermia ataxia

Introduction: Erythrokeratodermia ataxia

Description of Erythrokeratodermia ataxia

Erythrokeratodermia ataxia (medical condition): A rare inherited condition characterized by skin...more »

See also:

Erythrokeratodermia ataxia:
  »Introduction: Erythrokeratodermia ataxia
  »Symptoms of Erythrokeratodermia ataxia

Erythrokeratodermia ataxia: Related Topics

These medical condition or symptom topics may be relevant to medical information for Erythrokeratodermia ataxia:

Erythrokeratodermia ataxia: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

Erythrokeratodermia ataxia is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Erythrokeratodermia ataxia, or a subtype of Erythrokeratodermia ataxia, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)


Ophanet, a consortium of European partners, currently defines a condition rare when if affects 1 person per 2,000. They list Erythrokeratodermia ataxia as a "rare disease".

Source - Orphanet

Erythrokeratodermia ataxia as a Disease

Erythrokeratodermia ataxia (medical condition): See Erythrokeratodermia ataxia (disease information).
  »Introduction: Erythrokeratodermia ataxia
  »Symptoms of Erythrokeratodermia ataxia

Erythrokeratodermia ataxia: Related Diseases

Erythrokeratodermia ataxia: Erythrokeratodermia ataxia is listed as a type of (or associated with) the following medical conditions in our database:

More information on medical condition: Erythrokeratodermia ataxia:

Erythrokeratodermia ataxia: Related Disease Topics

These medical disease topics may be related to Erythrokeratodermia ataxia:

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