搜索结果
疾病ID:TCMBANKDI024118
疾病名:Congenital Amaurosis of Retinal Origin
MeSH_Name:Eye Diseases
HPO_Name:-
UMLS_Name:Disease or Syndrome
DO_Name:-
疾病类型:disease
DisGeNET_Link:C3540662
MeSH_Link:C11
HPO_Link:-
UMLS_Link:T047
DO_Link:-
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 |
|---|
| TCMBANKGE009285 | NMNAT1 | LCA9; NMNAT; PNAT1 | nicotinamide nucleotide adenylyltransferase 1 |
| TCMBANKGE006190 | SPATA7 | HEL-S-296; HSD-3.1; HSD3; LCA3 | spermatogenesis associated 7 |
| TCMBANKGE014361 | LRAT | LCA14 | lecithin retinol acyltransferase |
| TCMBANKGE004101 | RPE65 | BCO3; LCA2; RP20; mRPE65; p63; rd12; sRPE65 | retinoid isomerohydrolase RPE65 |
| TCMBANKGE008696 | IMPDH1 | IMPD; IMPD1; IMPDH-I; LCA11; RP10; sWSS2608 | inosine monophosphate dehydrogenase 1 |
| TCMBANKGE001871 | RPGRIP1 | CORD13; LCA6; RGI1; RGRIP; RPGRIP; RPGRIP1d | RPGR interacting protein 1 |
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Dai SX Lab