alkaptonuria (Q651680)
Jump to navigation
Jump to search
amino acid metabolic disorder that involves phenylalanine and tyrosine metabolism with the accumulation of homogentisic acid, a toxic tyrosine byproduct
- Homogentisate 1,2-dioxygenase deficiency
- alcaptonuria
- deficiency of homogentisicase
- Homogentisic Acid Oxidase Deficiency
- AKU
- Alkaptonuric ochronosis
- ochronosis, hereditary
- hereditary ochronosis
- homogentisic acidura
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | alkaptonuria |
amino acid metabolic disorder that involves phenylalanine and tyrosine metabolism with the accumulation of homogentisic acid, a toxic tyrosine byproduct |
|
Statements
2 references
1 reference
1 reference
1 reference
6 references
270.2
1 reference
C84546
2 references
1 reference
Alkaptonuria
0 references
Identifiers
Alkaptonuria
1 reference
1 reference
2 references
2 references
1 reference
1 reference
1 reference
Sitelinks
Wikipedia(23 entries)
- arwiki بيلة ألكابتونية
- bswiki Alkaptonurija
- ckbwiki نەخۆشی میزی ڕەش
- dewiki Alkaptonurie
- enwiki Alkaptonuria
- eswiki Alcaptonuria
- fawiki بیماری ادرار سیاه
- fiwiki Alkaptonuria
- frwiki Alcaptonurie
- huwiki Alkaptonuria
- itwiki Alcaptonuria
- jawiki アルカプトン尿症
- nlwiki Alkaptonurie
- plwiki Alkaptonuria
- ptwiki Alcaptonúria
- rowiki Alcaptonurie
- ruwiki Алкаптонурия
- skwiki Alkaptonúria
- slwiki Alkaptonurija
- srwiki Алкаптонурија
- svwiki Alkaptonuri
- thwiki แอลแคปโทนิวเรีย
- zhwiki 黑尿症
Wikibooks(0 entries)
Wikinews(0 entries)
Wikiquote(0 entries)
Wikisource(0 entries)
Wikiversity(0 entries)
Wikivoyage(0 entries)
Wiktionary(0 entries)
Multilingual sites(1 entry)
- commonswiki Category:Alkaptonuria