搜索结果
疾病ID:TCMBANKDI015963
疾病名:AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 1
MeSH_Name:Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases
HPO_Name:-
UMLS_Name:Disease or Syndrome
DO_Name:genetic disease; disease of anatomical entity
疾病类型:disease
DisGeNET_Link:C1845052
MeSH_Link:C16; C07
HPO_Link:-
UMLS_Link:T047
DO_Link:DOID:630; 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 |
|---|
| TCMBANKGE000066 | YY1 | DELTA; GADEVS; INO80S; NF-E1; UCRBP; YIN-YANG-1 | YY1 transcription factor |
| TCMBANKGE006832 | IGHG3 | IgG3 | immunoglobulin heavy constant gamma 3 (G3m marker) |
| TCMBANKGE000109 | ACTB | BRWS1; PS1TP5BP1 | actin beta |
| TCMBANKGE002000 | CTLA4 | ALPS5; CD; CD152; CELIAC3; CTLA-4; GRD4; GSE; IDDM12 | cytotoxic T-lymphocyte associated protein 4 |
| TCMBANKGE001223 | SLC17A5 | AST; ISSD; NSD; SD; SIALIN; SIASD; SLD | solute carrier family 17 member 5 |
| TCMBANKGE000498 | TBX21 | T-PET; T-bet; TBET; TBLYM | T-box transcription factor 21 |
滇IICP备16009434号-1 |
Dai SX Lab