trimethylaminuria
rare metabolic disorder
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trimethylaminuria
Summary
trimethylaminuria is a rare disease[1]. trimethylaminuria has Wikipedia articles in 18 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- trimethylaminuria's instance of is recorded as rare disease[3].
- trimethylaminuria's instance of is recorded as inherited metabolic disorder[4].
- trimethylaminuria's instance of is recorded as autosomal recessive disease[5].
- trimethylaminuria's instance of is recorded as class of disease[6].
- trimethylaminuria is a type of autosomal recessive disease[7].
- trimethylaminuria is a type of inherited metabolic disorder[8].
- trimethylaminuria is a type of disease[9].
- trimethylaminuria's symptoms and signs is recorded as fetor[10].
- trimethylaminuria's health specialty is recorded as endocrinology[11].
- trimethylaminuria's genetic association is recorded as FMO3[12].
- trimethylaminuria's exact match is recorded as http://purl.obolibrary.org/obo/HP_0003614[13].
- trimethylaminuria's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_35056[14].
- trimethylaminuria's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080361[15].
- trimethylaminuria's exact match is recorded as http://identifiers.org/doid/DOID:0080361[16].
- trimethylaminuria's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].
Why It Matters
trimethylaminuria has Wikipedia articles in 18 language editions, a strong signal of global cultural recognition.[2] trimethylaminuria is known by 20 alternative names across languages and contexts.[18]