Tyrosinemia - CaLiGraph

Property	Value
rdf:type	Disorder included in newborn screening programs owl:NamedIndividual Skin condition Amino acid metabolism disorder Autosomal recessive disorder Cause of hypoglycemia MeSH code (C16) MeSH code (C18)
rdfs:label	Tyrosinemia
owl:sameAs	dbr:Tyrosinemia
prov:wasDerivedFrom	http://en.wikipedia.org/wiki/List_of_diseases_(O) http://en.wikipedia.org/wiki/List_of_diseases_(T) http://en.wikipedia.org/wiki/Congenital_disorders_of_amino_acid_metabolism http://en.wikipedia.org/wiki/List_of_disorders_included_in_newborn_screening_programs http://en.wikipedia.org/wiki/List_of_MeSH_codes_(C16) http://en.wikipedia.org/wiki/List_of_causes_of_hypoglycemia http://en.wikipedia.org/wiki/Category:Amino_acid_metabolism_disorders http://en.wikipedia.org/wiki/Category:Autosomal_recessive_disorders http://en.wikipedia.org/wiki/List_of_MeSH_codes_(C18) http://en.wikipedia.org/wiki/Proximal_renal_tubular_acidosis http://en.wikipedia.org/wiki/Chromosome_12 http://en.wikipedia.org/wiki/Chromosome_15 http://en.wikipedia.org/wiki/Keratoderma
skos:prefLabel	Tyrosinemia
skos:altLabel	Oculocutaneous tyrosinemia Tyrosinaemia type 1 Tyrosine-oxidase temporary deficiency Tyrosinemia I Tyrosinemia III hereditary tyrosinemia type 1 hereditary tyrosinemia type I tyrosinemia tyrosinemias
clgo:diseasesDB	13478
clgo:eMedicineSubject	ped
clgo:eMedicineTopic	2339
clgo:icd10	E70.2
clgo:icd9	270.2
clgo:meshId	D020176
clgo:omim	276700

About: clgr:Tyrosinemia