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n10http://caligraph.org/ontology/ICD-9_code_240%E2%80%93279:_endocrine,_nutritional_and_metabolic_diseases,
n8http://en.wikipedia.org/wiki/List_of_ICD-9_codes_240%E2%80%93279:_endocrine,_nutritional_and_metabolic_diseases,
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Subject Item
clgr:Trimethylaminuria
rdf:type
owl:NamedIndividual clgo:Rare_disease clgo:Inborn_error_of_metabolism n10:_and_immunity_disorders clgo:Autosomal_recessive_disorder
rdfs:label
Trimethylaminuria
owl:sameAs
dbr:Trimethylaminuria
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n5: n8:_and_immunity_disorders n9:Chromosome_1 n9:Simple_Mendelian_genetics_in_humans n9:Bad_breath n9:Oligogenic_inheritance n9:Human_genetics n9:Congenital_disorders_of_amino_acid_metabolism n12:Autosomal_recessive_disorders n12:Inborn_errors_of_metabolism n9:Intestinal_metabolic_bromhidrosis_syndrome n12:Rare_diseases
skos:prefLabel
Trimethylaminuria
skos:altLabel
trimethylaminuria disorder trimethylamines rare medical condition trimethylaminuria fish odour syndrome Fish Odor syndrome
clgo:diseasesDB
4835
clgo:geneReviewsId
NBK1103
clgo:geneReviewsName
Trimethylaminuria
clgo:icd10
E88.8
clgo:icd9
270.8
clgo:omim
602079
Subject Item
clgr:George_Preti
clgo:knownFor
clgr:Trimethylaminuria