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疾病ID:TCMBANKDI017507


疾病名:Ornithine carbamoyltransferase deficiency


MeSH_Name:Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases


HPO_Name:-


UMLS_Name:Disease or Syndrome


DO_Name:disease of metabolism; genetic disease


疾病类型:disease


DisGeNET_Link:C0268542


MeSH_Link:C16; C18; C10


HPO_Link:-


UMLS_Link:T047


DO_Link:DOID:0014667; DOID:630


HERB_ID:-


   疾病对应的植物
ID 拉丁名 药名 药用植物名 功能与主治 来源 药用部位 使用民族

   疾病对应的化合物
化合物ID 化合物名 别名 分子式 分子质量 Smiles

   疾病对应的靶点
靶点ID 基因名 基因别名 描述
TCMBANKGE003153 DMD BMD; CMD3B; DXS142; DXS164; DXS206; DXS230; DXS239; DXS268; DXS269; DXS270; DXS272; MRX85 dystrophin
TCMBANKGE000962 TFEB ALPHATFEB; BHLHE35; TCFEB transcription factor EB
TCMBANKGE003899 SLC25A15 D13S327; HHH; LNC-HC; ORC1; ORNT1 solute carrier family 25 member 15
TCMBANKGE006708 RPGR COD1; CORDX1; CRD; PCDX; RP15; RP3; XLRP3; orf15 retinitis pigmentosa GTPase regulator
TCMBANKGE001090 CYTB MTCYB cytochrome b
TCMBANKGE011438 OTC OCTD ornithine carbamoyltransferase
TCMBANKGE010842 TSPAN7 A15; CCG-B7; CD231; DXS1692E; MRX58; MXS1; TALLA-1; TM4SF2; TM4SF2b tetraspanin 7
TCMBANKGE010690 PLXNA2 OCT; PLXN2 plexin A2
TCMBANKGE009361 GPT AAT1; ALT1; GPT1 glutamic--pyruvic transaminase
TCMBANKGE003643 F7 SPCA coagulation factor VII
TCMBANKGE003230 CPS1 CPSASE1; PHN carbamoyl-phosphate synthase 1
TCMBANKGE004553 CYP21A2 CA21H; CAH1; CPS1; CYP21; CYP21B; P450c21B cytochrome P450 family 21 subfamily A member 2
TCMBANKGE006356 PM20D1 Cps1 peptidase M20 domain containing 1
TCMBANKGE005110 GLUL GLNS; GS; PIG43; PIG59 glutamate-ammonia ligase