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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tyrosinemia type II
Summary
tyrosinemia type II is a designated intractable/rare disease[1]. It draws 20 Wikipedia views per month (designated_intractable_rare_disease category, ranking #154 of 201).[2]
Key Facts
- tyrosinemia type II's instance of is recorded as designated intractable/rare disease[3].
- tyrosinemia type II's instance of is recorded as rare disease[4].
- tyrosinemia type II's instance of is recorded as class of disease[5].
- tyrosinemia type II's subclass of is recorded as tyrosinemia[6].
- tyrosinemia type II's subclass of is recorded as liver disease[7].
- tyrosinemia type II's subclass of is recorded as skin disease[8].
- tyrosinemia type II's OMIM ID is recorded as 276600[9].
- tyrosinemia type II's ICD-9 ID is recorded as 270.2[10].
- tyrosinemia type II's ICD-10 ID is recorded as E70.2[11].
- tyrosinemia type II's DiseasesDB is recorded as 13486[12].
- tyrosinemia type II's Disease Ontology ID is recorded as DOID:0050725[13].
- tyrosinemia type II's anatomical location is recorded as zone of skin[14].
- tyrosinemia type II's anatomical location is recorded as liver[15].
- tyrosinemia type II's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4693[16].
- tyrosinemia type II's Orphanet ID is recorded as 28378[17].
- tyrosinemia type II's NCI Thesaurus ID is recorded as C129032[18].
- tyrosinemia type II's health specialty is recorded as neurology[19].
- tyrosinemia type II's health specialty is recorded as medical genetics[20].
- tyrosinemia type II's health specialty is recorded as endocrinology[21].
- tyrosinemia type II's genetic association is recorded as TAT[22].
- tyrosinemia type II's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050725[23].
- tyrosinemia type II's exact match is recorded as http://identifiers.org/doid/DOID:0050725[24].
- tyrosinemia type II's PatientsLikeMe condition ID is recorded as tyrosinemia-type-ii[25].
- tyrosinemia type II's GARD rare disease ID is recorded as 3105[26].
- tyrosinemia type II's on focus list of Wikimedia project is recorded as WikiProject Medicine[27].
Why It Matters
tyrosinemia type II draws 20 Wikipedia views per month (designated_intractable_rare_disease category, ranking #154 of 201).[2] It is known by 9 alternative names across languages and contexts.[28]