tyrosinemia type II (Q7484623)
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tyrosinemia that has material basis in deficiency of hepatic tyrosine aminotransferase located in the liver and is characterized by keratitis, painful palmoplantar hyperkeratosis, mental retardation, and elevated serum tyrosine levels
- Oculocutaneous tyrosinemia
- Richner-Hanhart syndrome
- Hypertyrosinemia type II
- Tyrosinemia II
- Hereditary tyrosinemia, Type II
- TYRSN2
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | tyrosinemia type II |
tyrosinemia that has material basis in deficiency of hepatic tyrosine aminotransferase located in the liver and is characterized by keratitis, painful palmoplantar hyperkeratosis, mental retardation, and elevated serum tyrosine levels |
|
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17 May 2019
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C129032
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Wikipedia(5 entries)
- dvwiki ހޭންހާރޓް ސިންޑްރޯމް
- enwiki Tyrosinemia type II
- eswiki Tirosinemia tipo 2
- fawiki تیروزینمی نوع دو
- ttwiki 2 типтагы тирозинемия