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疾病ID:TCMBANKDI021886
疾病名:Complete congenital stationary night blindness
MeSH_Name:-
HPO_Name:Abnormality of the eye
UMLS_Name:Congenital Abnormality
DO_Name:-
疾病类型:disease
DisGeNET_Link:C4048798
MeSH_Link:-
HPO_Link:HP:0000478
UMLS_Link:T019
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 |
|---|
| TCMBANKGE009871 | GRM6 | CSNB1B; GPRC1F; MGLUR6; mGlu6 | glutamate metabotropic receptor 6 |
| TCMBANKGE008429 | CACNA1F | AIED; COD3; COD4; CORDX; CORDX3; CSNB2; CSNB2A; CSNBX2; Cav1.4; Cav1.4alpha1; JM8; JMC8; OA2 | calcium voltage-gated channel subunit alpha1 F |
| 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