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3q21-q23 GeneReviews Google OMIM Orphanet PubMed Wikipedia [Eyes] Alkaptonuria *Gene map locus 3q21-q23 AKU Homogentisic acid oxidase deficiency Ochronosis, hereditary [Clinical features: black urine disease; black ochronotic pigmentation of cartilage and collagenous tissues; ochronotic arthritis] [Inheritance: autosomal recessive] |
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Aortic Valve Stenosis in Alkaptonuria |
Aortic Valve Stenosis in Alkaptonuria |
Aortic Valve Stenosis in Alkaptonuria |
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Circulation |
Circulation |
Circulation |
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29 images [ from 1 to 15 ] |
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