KEGG MEDICUS 医薬品情報

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2738 件中 2401 〜 2440 を表示 前へ 1 ... 56 57 58 59 60 61 62 63 64 65 66 ... 69 次へ
エントリ 名称 カテゴリ パスウェイ 病因遺伝子
H02408 瓜実条虫症 寄生虫感染症
H02409 二腔吸虫感染症 寄生虫感染症
H02410 骨髄異形成/骨髄増殖性腫瘍 がん DNMT3A (mutation) [HSA:1788] [KO:K17398]
TET2 (mutation) [HSA:54790] [KO:K24309]
IDH1 (mutation) [HSA:3417] [KO:K00031]
IDH2 (mutation) [HSA:3418] [KO:K00031]
ASXL1 (mutation) [HSA:171023] [KO:K11471]
EZH2 (mutation) [HSA:2146] [KO:K11430]
NRAS (mutation) [HSA:4893] [KO:K07828]
KRAS (mutation) [HSA:3845] [KO:K07827]
JAK2 (mutation) [HSA:3717] [KO:K04447]
CBL (mutation) [HSA:867] [KO:K04707]
SETBP1 (mutation) [HSA:26040] [KO:K23217]
CSF3R (mutation) [HSA:1441] [KO:K05061]
PTPN11 (mutation) [HSA:5781] [KO:K07293]
NF1 (mutation) [HSA:4763] [KO:K08052]
SF3B1 (mutation) [HSA:23451] [KO:K12828]
SRSF2 (mutation) [HSA:6427] [KO:K12891]
U2AF1 (mutation) [HSA:7307] [KO:K12836]
ZRSR2 (mutation) [HSA:8233] [KO:K24273]
RUNX1 (mutation) [HSA:861] [KO:K08367]
CEBPA (mutation) [HSA:1050] [KO:K09055]
H02411 慢性骨髄単球性白血病 がん TET2 (mutation) [HSA:54790] [KO:K24309]
ASXL1 (mutation) [HSA:171023] [KO:K11471]
SRSF2 (mutation) [HSA:6427] [KO:K12891]
NRAS (mutation) [HSA:4893] [KO:K07828]
KRAS (mutation) [HSA:3845] [KO:K07827]
CBL (mutation) [HSA:867] [KO:K04707]
RUNX1 (mutation) [HSA:861] [KO:K08367]
SF3B1 (mutation) [HSA:23451] [KO:K12828]
ZRSR2 (mutation) [HSA:8233] [KO:K24273]
U2AF1 (mutation) [HSA:7307] [KO:K12836]
DNMT3A (mutation) [HSA:1788] [KO:K17398]
EZH2 (mutation) [HSA:2146] [KO:K11430]
TP53 (mutation) [HSA:7157] [KO:K04451]
NPM1 (mutation) [HSA:4869] [KO:K11276]
JAK2 (mutation) [HSA:3717] [KO:K04447]
FLT3 (mutation) [HSA:2322] [KO:K05092]
H02412 非定型慢性骨髄性白血病 がん SETBP1 (mutation) [HSA:26040] [KO:K23217]
NRAS (mutation) [HSA:4893] [KO:K07828]
KRAS (mutation) [HSA:3845] [KO:K07827]
JAK2 (mutation) [HSA:3717] [KO:K04447]
CSF3R (mutation) [HSA:1441] [KO:K05061]
ASXL1 (mutation) [HSA:171023] [KO:K11471]
ETNK1 (mutation) [HSA:55500] [KO:K00894]
TET2 (mutation) [HSA:54790] [KO:K24309]
SRSF2 (mutation) [HSA:6427] [KO:K12891]
EZH2 (mutation) [HSA:2146] [KO:K11430]
RUNX1 (mutation) [HSA:861] [KO:K08367]
CBL (mutation) [HSA:867] [KO:K04707]
FLT3 (mutation) [HSA:2322] [KO:K05092]
CEBPA (mutation) [HSA:1050] [KO:K09055]
IDH2 (mutation) [HSA:3418] [KO:K00031]
H02413 流行性筋痛症
流行性胸痛症
ボルンホルム病 		ウイルス感染症
H02414 自己炎症性疾患・脂肪織炎および皮膚疾患症候群 免疫系疾患 OTULIN [HSA:90268] [KO:K18343]
H02415 頭蓋顔面異形症・骨格異常・精神遅滞症候群 先天奇形 (CFSMR1) TMCO1 [HSA:54499] [KO:K21891]
(CFSMR2) RAB5IF [HSA:55969] [KO:K26496]
H02416 トコジラミ症 寄生虫感染症
H02417 多毛症を伴う歯肉増殖症 先天奇形 ABCA5 [HSA:23461] [KO:K05648]
H02418 非ホジキンリンパ腫 がん RAD54L [HSA:8438] [KO:K10875]
RAD54B [HSA:25788] [KO:K10877]
CASP10 [HSA:843] [KO:K04400]
PRF1 [HSA:5551] [KO:K07818]
H02419 血清グリシン濃度正常のグリシン脳症 先天性代謝異常症 SLC6A9 [HSA:6536] [KO:K05038]
H02420 頭頸部癌 がん
H02421 固形腫瘍
固形癌 		がん
H02422 骨格奇形を伴う網膜色素変性 先天奇形 CWC27 [HSA:10283] [KO:K12737]
H02423 ケジラミ症 寄生虫感染症
H02424 中枢神経系原発悪性リンパ腫 がん MYD88 (mutation) [HSA:4615] [KO:K04729]
CD79B (mutation) [HSA:974] [KO:K06507]
CARD11 (mutation) [HSA:84433] [KO:K07367]
TNFAIP3 (mutation) [HSA:7128] [KO:K11859]
HLA-DRB5 (deletion) [HSA:3127] [KO:K06752]
CDKN2A (deletion) [HSA:1029] [KO:K06621]
H02425 エルドハイム・チェスター病 がん BRAF (mutation) [HSA:673] [KO:K04365]
MAP2K1 (mutation) [HSA:5604] [KO:K04368]
ARAF (mutation) [HSA:369] [KO:K08845]
MAP2K2 (mutation) [HSA:5605] [KO:K04369]
KRAS (mutation) [HSA:3845] [KO:K07827]
NRAS (mutation) [HSA:4893] [KO:K07828]
H02426 EDICT 症候群 先天奇形 MIR184 [HSA:406960] [KO:K17177]
H02427 軟部肉腫 がん
H02428 トリコスポロン症 真菌感染症
H02429 日光角化症 皮膚疾患
H02430 難聴と糖尿病を伴う小脳および末梢性複合運動失調 神経系疾患 DNAJC3 [HSA:5611] [KO:K09523]
H02431 小脳低形成、てんかん、および全般的発達遅滞 先天奇形 OXR1 [HSA:55074] [KO:K25437]
H02432 ブチリルコリンエステラーゼ欠損症 先天性代謝異常症 BCHE [HSA:590] [KO:K01050]
H02433 脳幹および脊髄の障害と下肢痙縮を伴う髄鞘低形成 先天性代謝異常症 DARS1 [HSA:1615] [KO:K22503]
H02434 びまん性大細胞型B細胞リンパ腫、非特定 がん EZH2 (mutation) [HSA:2146] [KO:K11430]
CREBBP (mutation/deletion) [HSA:1387] [KO:K04498]
EP300 (mutation/deletion) [HSA:2033] [KO:K04498]
GNA13 (mutation) [HSA:10672] [KO:K04639]
GNAI2 (mutation) [HSA:2768] [KO:K04346]
TNFRSF14 (mutation) [HSA:8764] [KO:K05152]
BCL6 (mutation) [HSA:604] [KO:K15618]
MYC (chromosomal translocation) [HSA:4609] [KO:K04377]
PTEN (deletion) [HSA:5728] [KO:K01110]
BCL2 (chromosomal translocation / mutation) [HSA:596] [KO:K02161]
CARD11 (mutation) [HSA:84433] [KO:K07367]
CD79A (mutation) [HSA:973] [KO:K06506]
CD79B (mutation) [HSA:974] [KO:K06507]
TNFAIP3 (mutation/deletion) [HSA:7128] [KO:K11859]
MYD88 (mutation) [HSA:4615] [KO:K04729]
CDKN2A (deletion) [HSA:1029] [KO:K06621]
CDKN2B (deletion) [HSA:1030] [KO:K04685]
PRDM1 (mutation/deletion) [HSA:639] [KO:K24501]
MLL2 (mutation) [HSA:8085] [KO:K09187]
MLL3 (mutation) [HSA:58508] [KO:K09188]
B2M (mutation/deletion) [HSA:567] [KO:K08055]
CD58 (mutation/deletion) [HSA:965] [KO:K06492]
TP53 (mutation) [HSA:7157] [KO:K04451]
MEF2B (mutation) [HSA:100271849] [KO:K09261]
FOXO1 (mutation) [HSA:2308] [KO:K07201]
H02435 難聴-不妊症候群 先天奇形 CATSPER2 [HSA:117155] [KO:K16890]
STRC [HSA:161497] [KO:K24636]
H02436 Al-Gazali 症候群 先天奇形 B3GALT6 [HSA:126792] [KO:K00734]
H02437 成長遅滞、知的発達障害、筋緊張低下および肝障害 先天奇形 IARS1 [HSA:3376] [KO:K01870]
H02438 高グリシン血症、乳酸アシドーシスおよび痙攣 先天性代謝異常症 LIAS [HSA:11019] [KO:K03644]
H02439 低身長、成長遅滞、先天性心疾患 先天性代謝異常症 TKT [HSA:7086] [KO:K00615]
H02440 家族性良性斑点網膜症 神経系疾患 PLA2G5 [HSA:5322] [KO:K01047]
H02441 HUPRA 症候群 先天性代謝異常症 SARS2 [HSA:54938] [KO:K01875]
H02442 風邪
普通感冒 		ウイルス感染症
H02444 Luscan-Lumish 症候群 先天奇形 SETD2 [HSA:29072] [KO:K11423]
H02445 小角膜・近視性網脈絡膜萎縮および眼角隔離 先天奇形 ADAMTS18 [HSA:170692] [KO:K08632]
H02446 常染色体劣性遺伝性巨頭症/巨脳症症候群 先天奇形 TBC1D7 [HSA:51256] [KO:K20396]
H02447 錐体外路症状を伴うミオパチー 神経系疾患 MICU1 [HSA:10367] [KO:K22827]
H02448 Harel-Yoon 症候群 神経系疾患 ATAD3A [HSA:55210] [KO:K17681]
2738 件中 2401 〜 2440 を表示 前へ 1 ... 56 57 58 59 60 61 62 63 64 65 66 ... 69 次へ
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