tyrosinemia type III
tyrosinemia that has material basis in deficiency of 4-hydroxyphenylpyruvate dioxygenase disrupting the break down of tyrosine
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tyrosinemia type III
Summary
tyrosinemia type III is a designated intractable/rare disease[1]. It draws 3 Wikipedia views per month (designated_intractable_rare_disease category, ranking #167 of 201).[2]
Key Facts
- tyrosinemia type III's instance of is recorded as designated intractable/rare disease[3].
- tyrosinemia type III's instance of is recorded as rare disease[4].
- tyrosinemia type III's instance of is recorded as class of disease[5].
- tyrosinemia type III's subclass of is recorded as tyrosinemia[6].
- tyrosinemia type III's OMIM ID is recorded as 276710[7].
- tyrosinemia type III's ICD-9 ID is recorded as 270.2[8].
- tyrosinemia type III's ICD-10 ID is recorded as E70.2[9].
- tyrosinemia type III's DiseasesDB is recorded as 29836[10].
- tyrosinemia type III's Disease Ontology ID is recorded as DOID:0050727[11].
- tyrosinemia type III's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4696[12].
- tyrosinemia type III's Orphanet ID is recorded as 69723[13].
- tyrosinemia type III's health specialty is recorded as endocrinology[14].
- tyrosinemia type III's drug or therapy used for treatment is recorded as nitisinone[15].
- tyrosinemia type III's drug or therapy used for treatment is recorded as sodium ascorbate[16].
- tyrosinemia type III's genetic association is recorded as HPD[17].
- tyrosinemia type III's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050727[18].
- tyrosinemia type III's exact match is recorded as http://identifiers.org/doid/DOID:0050727[19].
- tyrosinemia type III's PatientsLikeMe condition ID is recorded as tyrosinemia-type-iii[20].
- tyrosinemia type III's GARD rare disease ID is recorded as 10332[21].
- tyrosinemia type III's on focus list of Wikimedia project is recorded as WikiProject Medicine[22].
- tyrosinemia type III's Mondo ID is recorded as MONDO_0010162[23].
- tyrosinemia type III's Microsoft Academic ID is recorded as 2775904740[24].
- tyrosinemia type III's has phenotype is recorded as Hypertyrosinemia[25].
- tyrosinemia type III's UniProt disease ID is recorded as DI-01109[26].
Why It Matters
tyrosinemia type III draws 3 Wikipedia views per month (designated_intractable_rare_disease category, ranking #167 of 201).[2]