3-Methylcrotonyl-CoA carboxylase deficiency

Property	Value
rdf:type	Disorder included in newborn screening programs owl:NamedIndividual Amino acid metabolism disorder Autosomal recessive disorder Cause of hypoglycemia
rdfs:label	3-Methylcrotonyl-CoA carboxylase deficiency
owl:sameAs	dbr:3-Methylcrotonyl-CoA_carboxylase_deficiency
prov:wasDerivedFrom	http://en.wikipedia.org/wiki/Chromosome_3 http://en.wikipedia.org/wiki/Chromosome_5 http://en.wikipedia.org/wiki/List_of_diseases_(0%E2%80%939) http://en.wikipedia.org/wiki/List_of_disorders_included_in_newborn_screening_programs 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/Hypotonia
skos:prefLabel	3-Methylcrotonyl-CoA carboxylase deficiency
skos:altLabel	3-methyl crotonyl-coa carboxylase deficiency Beta-methyl crotonyl carboxylase deficiency MCC-deficient syndrome
clgo:diseasesDB	32207
clgo:omim	210200

About: clgr:3-Methylcrotonyl-CoA_carboxylase_deficiency