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疾病ID:TCMBANKDI025624
疾病名:Syndactyly, type 2
MeSH_Name:Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
HPO_Name:-
UMLS_Name:Congenital Abnormality
DO_Name:disease of anatomical entity
疾病类型:disease
DisGeNET_Link:C2699746
MeSH_Link:C16; C05
HPO_Link:-
UMLS_Link:T019
DO_Link:DOID:7
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 |
|---|
| TCMBANKGE000897 | GLI3 | ACLS; GCPS; GLI3-190; GLI3FL; PAP-A; PAPA; PAPA1; PAPB; PHS; PPDIV | GLI family zinc finger 3 |
| TCMBANKGE012163 | HOXD8 | HOX4; HOX4E; HOX5.4 | homeobox D8 |
| TCMBANKGE012078 | FBLN1 | FBLN; FIBL1 | fibulin 1 |
| TCMBANKGE003770 | KIF1B | CMT2; CMT2A; CMT2A1; HMSNII; KLP; NBLST1 | kinesin family member 1B |
| TCMBANKGE008936 | IFT122 | CED; CED1; FAP80; SPG; WDR10; WDR10p; WDR140 | intraflagellar transport 122 |
| TCMBANKGE011362 | HOXA13 | HOX1; HOX1J | homeobox A13 |
| TCMBANKGE015059 | TTC30B | IFT70; IFT70B; fleer | tetratricopeptide repeat domain 30B |
| TCMBANKGE008735 | WDR19 | ATD5; CED4; DYF-2; FAP66; IFT144; NPHP13; ORF26; Oseg6; PWDMP; SRTD5 | WD repeat domain 19 |
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Dai SX Lab