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疾病ID:TCMBANKDI003384
疾病名:Optic atrophy from cranial nerve compression
MeSH_Name:Eye Diseases; Nervous System Diseases
HPO_Name:Abnormality of the nervous system; Abnormality of the eye
UMLS_Name:Pathologic Function
DO_Name:-
疾病类型:phenotype
DisGeNET_Link:C4024763
MeSH_Link:C11; C10
HPO_Link:HP:0000707; HP:0000478
UMLS_Link:T046
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 |
|---|
| TCMBANKGE005314 | SOST | CDD; DAND6; SOST1; VBCH | sclerostin |
| TCMBANKGE012674 | PLEKHM1 | AP162; B2; OPTA3; OPTB6 | pleckstrin homology and RUN domain containing M1 |
| TCMBANKGE012909 | CLCN7 | CLC-7; CLC7; HOD; OPTA2; OPTB4; PPP1R63 | chloride voltage-gated channel 7 |
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