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*142940 - 3-@HYDROXY-3-METHYLGLUTARYL-CoA SYNTHASE 1; HMGCS1
Gene summaries Genetic tests Medical literature
*615804 - UREIDOIMIDAZOLINE (2-OXO-4-HYDROXY-4-CARBOXY-5-) DECARBOXYLASE; URAD
Cytogenetic locations: 16462750
237000 - HYDROXYPROLINEMIA
*619050 - 3-@HYDROXY-3-METHYLGLUTARYL-CoA LYASE-LIKE PROTEIN 1; HMGCLL1
Cytogenetic locations: 22865860
#607765 - BILE ACID SYNTHESIS DEFECT, CONGENITAL, 1; CBAS1
Cytogenetic locations: 17.1-8.7
#605911 - 3-@HYDROXY-3-METHYLGLUTARYL-CoA SYNTHASE-2 DEFICIENCY; HMGCS2D
Cytogenetic locations: 39337379
#246450 - 3-@HYDROXY-3-METHYLGLUTARYL-CoA LYASE DEFICIENCY; HMGCLD
Cytogenetic locations: 36228350
*600234 - 3-@HYDROXY-3-METHYLGLUTARYL-CoA SYNTHASE 2; HMGCS2
Cytogenetic locations: 12647205
*607764 - 3-@BETA-HYDROXY-DELTA-5-C27-STEROID OXIDOREDUCTASE; HSD3B7
*613597 - 4-@HYDROXY-2-OXOGLUTARATE ALDOLASE 1; HOGA1
Cytogenetic locations: mutation
*613898 - 3-@HYDROXY-3-METHYLGLUTARYL-CoA LYASE; HMGCL
*142910 - 3-@HYDROXY-3-METHYLGLUTARYL-CoA REDUCTASE; HMGCR
Cytogenetic locations: 171833
#609016 - LONG-CHAIN 3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY
Cytogenetic locations: Wdcp
#613812 - BILE ACID SYNTHESIS DEFECT, CONGENITAL, 3; CBAS3
Cytogenetic locations: 18367963
#617671 - HELIX SYNDROME; HELIX
Cytogenetic locations: 28686597
#250620 - 3-@HYDROXYISOBUTYRYL-CoA HYDROLASE DEFICIENCY; HIBCHD
Cytogenetic locations: 26026795
#239510 - HYPERPROLINEMIA, TYPE II; HYRPRO2
Cytogenetic locations: 10780262
#613616 - HYPEROXALURIA, PRIMARY, TYPE III; HP3
#620375 - MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 28; LGMDR28
*614811 - L-3-HYDROXYPROLINE DEHYDRATASE, TRANS; L3HYPDH
Cytogenetic locations: 22528483
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