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Gunther's disease

Introduction: Gunther's disease

Description of Gunther's disease

Gunther's disease: An autosomal recessive porphyria that is due to a deficiency of UROPORPHYRINOGEN III SYNTHASE in the BONE MARROW; also known as congenital erythropoietic porphyria. This disease is characterized by SPLENOMEGALY; ANEMIA; photosensitivity; cutaneous lesions; accumulation of hydroxymethylbilane; and increased excretion of UROPORPHYRINS and COPROPORPHYRINS.
Source: Diseases Database

Gunther's disease: Related Topics

These medical condition or symptom topics may be relevant to medical information for Gunther's disease:

Terms associated with Gunther's disease:

Terms Similar to Gunther's disease:

Source: Diseases Database

The following terms can be used for Gunther's disease

Source: CRISP

External links related to: Gunther's disease

Source: Diseases Database

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