搜索结果
疾病ID:TCMBANKDI016758
疾病名:Night Blindness, Congenital Stationary, Type 1A
MeSH_Name:Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
HPO_Name:-
UMLS_Name:Disease or Syndrome
DO_Name:genetic disease; disease of anatomical entity
疾病类型:disease
DisGeNET_Link:C3495587
MeSH_Link:C16; C11
HPO_Link:-
UMLS_Link:T047
DO_Link:DOID:630; DOID:7
HERB_ID:HBDIS021514
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 |
|---|
| TCMBANKGE014420 | GNB3 | CSNB1H | G protein subunit beta 3 |
| TCMBANKGE009871 | GRM6 | CSNB1B; GPRC1F; MGLUR6; mGlu6 | glutamate metabotropic receptor 6 |
| TCMBANKGE012594 | RHO | CSNBAD1; OPN2; RP4 | rhodopsin |
| TCMBANKGE007866 | SAG | RP47; S-AG | S-antigen visual arrestin |
| TCMBANKGE008429 | CACNA1F | AIED; COD3; COD4; CORDX; CORDX3; CSNB2; CSNB2A; CSNBX2; Cav1.4; Cav1.4alpha1; JM8; JMC8; OA2 | calcium voltage-gated channel subunit alpha1 F |
| TCMBANKGE001687 | PDE6B | CSNB3; CSNBAD2; GMP-PDEbeta; PDEB; RP40; rd1 | phosphodiesterase 6B |
| TCMBANKGE010690 | PLXNA2 | OCT; PLXN2 | plexin A2 |
| TCMBANKGE007470 | SLC24A1 | CSNB1D; HsT17412; NCKX; NCKX1; RODX | solute carrier family 24 member 1 |
| TCMBANKGE012213 | TRPM1 | CSNB1C; LTRPC1; MLSN1 | transient receptor potential cation channel subfamily M member 1 |
| TCMBANKGE010558 | NYX | CLRP; CSNB1; CSNB1A; CSNB4; NBM1 | nyctalopin |
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Dai SX Lab