| Ochronosis, (Alkaptonuria) | |
| Rare recessive metabolic disease with missing homogentisic acid oxidase with deposit of pigmented metabolic byproducts in sclera, cornea and conjunctiva and elsewhere in the body. | |
| Wollensak, Josef, Prof. Dr. med., Univ.-Augenklinik, Berlin, Germany | |
| E70.2 | |
| Systemic Diseases -> Metabolic Diseases -> Protein Metabolism -> Amino-acid Disturbances -> Primary -> Ochronosis | |
| sclera; conjunctiva; congenital metabolic disease | |
| 2655 |
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Ochronosis, (Alkaptonuria)-------------------------- -------------------------- -------------------------- -------------------------- -------------------------- -------------------------- -------------------------- -------------------------- -------------------------- -------------------------- -------------------------- -------------------------- |
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