tyrosinemia type III (Q7861692)
Jump to navigation
Jump to search
tyrosinemia that has material basis in deficiency of 4-hydroxyphenylpyruvate dioxygenase disrupting the break down of tyrosine
- Hypertyrosinemia type III
- Hereditary tyrosinemia, Type III
- High tyrosinemia
- TYRSN3
Language | Label | Description | Also known as |
---|---|---|---|
English | tyrosinemia type III |
tyrosinemia that has material basis in deficiency of 4-hydroxyphenylpyruvate dioxygenase disrupting the break down of tyrosine |
|
Statements
1 reference
17 May 2019
1 reference
1 reference
1 reference
2 references
1 reference
Identifiers
1 reference
1 reference
Sitelinks
Wikipedia(3 entries)
- enwiki Tyrosinemia type III
- eswiki Tirosinemia tipo 3
- fawiki تیروزینمی نوع سه