Search Result |
Top |
| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H00535 | Lymphatic malformation | Lymphatic malformation (LMPHM), formerly known as hereditary lymphedema (LMPH), is a form of generalized lymphatic dysplasia characterized by chronic lesions of the extremities due to insufficient lymphatic ... | Congenital malformation |
(LMPHM1/LMPH1A) FLT4 [HSA:2324] [KO:K05097] (LMPHM3/LMPH1C) GJC2 [HSA:57165] [KO:K07619] (LMPHM4/LMPH1D) VEGFC [HSA:7424] [KO:K05449] (LMPHM6/LMPH3) PIEZO1 [HSA:9780] [KO:K22128] (LMPHM7) EPHB4 [HSA:2050] [KO:K05113] (LMPHM8) CALCRL [HSA:10203] [KO:K04577] (LMPHM9) CELSR1 [HSA:9620] [KO:K04600] (LMPHM10) ANGPT2 [HSA:285] [KO:K05466] (LMPHM11) TIE1 [HSA:7075] [KO:K05120] (LMPHM12) MDFIC [HSA:29969] (LMPHM13) THSD1 [HSA:55901] [KO:K24433] (LMPHM14) ERG [HSA:2078] [KO:K09435] |
|
| H01593 | Osteoporosis | Osteoporosis is a common disease characterised by a generalised reduction in bone mineral density (BMD), microarchitectural deterioration of bone tissue and an increased risk of fracture. Since BMD values ... | Musculoskeletal disease |
(BMND1) LRP5 [HSA:4041] [KO:K03068] (BMND12) UGT2B17 [HSA:7367] [KO:K00699] (BMND15) MIR2861 [HSA:100422910] (BMND16) WNT1 [HSA:7471] [KO:K03209] (BMND17) LGR4 [HSA:55366] [KO:K04309] (BMND18) PLS3 [HSA:5358] [KO:K17336] (OPDD) COPB2 [HSA:9276] [KO:K17302] PDLIM4 [HSA:8572] [KO:K23353] CALCR [HSA:799] [KO:K04576] COL1A1 [HSA:1277] [KO:K06236] COL1A2 [HSA:1278] [KO:K06236] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |