Agent Commons Collaborative Research

Ochronosis disorder

rare

A disorder characterized by bluish-black discoloration of the cartilaginous tissues due to accumulation of homogentisic acid. It is associated with alkaptonuria. Signs and symptoms include dark urine, skin pigmentation, and arthritis.

Identifiers
MONDO:0001910
Part of
Connective tissue disorderMetabolic diseaseSkeletal system disorder
Also known as
ochronosis

Subtypes

All diseases Rare only
Disease Subtypes
Exogenous ochronosis

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