alkaptonuria
amino acid metabolic disorder that involves phenylalanine and tyrosine metabolism with the accumulation of homogentisic acid, a toxic tyrosine byproduct
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alkaptonuria
Summary
alkaptonuria is a rare disease[1]. alkaptonuria has Wikipedia articles in 19 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- alkaptonuria's instance of is recorded as rare disease[3].
- alkaptonuria's instance of is recorded as class of disease[4].
- alkaptonuria is a type of amino acid metabolic disorder[5].
- alkaptonuria is a type of tyrosinemia[6].
- alkaptonuria is a type of other metabolic disease with skin involvement[7].
- alkaptonuria is a type of pigmented conjunctival lesion[8].
- alkaptonuria is a type of disease[9].
- alkaptonuria's Commons category is recorded as Alkaptonuria[10].
- alkaptonuria's ICD-9-CM is recorded as 270.2[11].
- alkaptonuria's NCI Thesaurus ID is recorded as C84546[12].
- alkaptonuria's health specialty is recorded as endocrinology[13].
- alkaptonuria's genetic association is recorded as HGD[14].
- alkaptonuria's exact match is recorded as http://purl.obolibrary.org/obo/DOID_9270[15].
- alkaptonuria's exact match is recorded as http://identifiers.org/doid/DOID:9270[16].
- alkaptonuria's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_56[17].
- alkaptonuria's on focus list of Wikimedia project is recorded as WikiProject Medicine[18].
Why It Matters
alkaptonuria has Wikipedia articles in 19 language editions, a strong signal of global cultural recognition.[2] alkaptonuria is known by 16 alternative names across languages and contexts.[19]