Network variation - Cholesterol biosynthesis |
ENTRY | nt06034 |
Name | Cholesterol biosynthesis |
Category | Pathway view; Lipid/glycolipid metabolism |
Pathway | hsa00900 Terpenoid backbone biosynthesis hsa00100 Steroid biosynthesis |
Module | hsa_M00095 C5 isoprenoid biosynthesis, mevalonate pathway hsa_M00367 C10-C20 isoprenoid biosynthesis, non-plant eukaryotes hsa_M00101 Cholesterol biosynthesis, FPP => cholesterol hsa_M00103 Cholecalciferol biosynthesis |
Display | drug-target relation disease type |
Disease name | Disease category | ||
MEVA/POROK3 | H00206 | Mevalonate kinase deficiency | Inherited metabolic disorder |
H01933 | Porokeratosis | Congenital malformation | |
POROK1 | H01933 | Porokeratosis | Congenital malformation |
POROK7 | H01933 | Porokeratosis | Congenital malformation |
POROK9 | H01933 | Porokeratosis | Congenital malformation |
APMR4 | H02303 | Alopecia-mental retardation syndrome | Congenital malformation |
GRBGD | H00447 | HEM skeletal dysplasia | Congenital malformation |
MCCPD | H02132 | Microcephaly syndrome | Congenital malformation |
CHILD/CKS | H00496 | Congenital hemidysplasia with ichthyosiform nevus and limb defects (CHILD) | Congenital malformation |
H01917 | CK syndrome | Congenital malformation | |
Desmosterolosis | H00617 | Desmosterolosis | Inherited metabolic disorder |
CDPX2/MEND | H01194 | X-linked chondrodysplasia punctata | Congenital malformation |
H02248 | MEND syndrome | Congenital malformation | |
LATHOS | H01281 | Lathosterolosis | Inherited metabolic disorder |
SLOS | H00161 | Smith-Lemli-Opitz syndrome | Inherited metabolic disorder |
VDDR1B | H01143 | Vitamin D-dependent rickets | Inherited metabolic disorder |
VDDR1A | H01143 | Vitamin D-dependent rickets | Inherited metabolic disorder |