|
DOID:0014667 - disease of metabolism
Disease Ontology Definition:A disease that involving errors in metabolic processes of building or degradation of molecules.
Synonyms: metabolic disease ,
Echinobase Genes : alg12, cog8, ppox, etfb, hmbs, sdhd, nfu1, hadh, ppm1k, adk, mttp, Tcf/Lef, ttc19, hgsnat, alg11, [+]
ephx2, asah1, etfdh, slc16a1, aga, alg8, gm2a, agk, coq2, asah1, tmem165, pcca, cog7, mccc1, mpdu1,
ears2, cog6, pccb, acadvl, bcs1l, mpi, alg9, gfm1, sucla2, pex1, lmbrd1, gale, tpmt, ppt1, abat,
cox10, lmf1, uqcrc2, atpaf2, slc35a1, sgsh, gck, gne, serac1, mogs, hoga1, mgat2, cox15, agxt, mrps22,
manba, sco1, ddost, d2hgdh, alg3, tymp, LOC100892337, gnptab, pdhx, pex16, twnk, hprt1, phgdh, mmut, fbxl4,
neurod1, mmadhc, taco1, mmab, mrpl44, pex12, asl, tufm, ctsd, rmnd1, slc25a1, hnf1a, hpd, acads, gbe1,
slc37a4, acat1, hlcs, pex7, otc, LOC752050, cpox, ldlrap1, slc17a5, mmachc, dpyd, glis3, urod, LOC581408, agl,
cth, alg6, dbt, gldc, dpm2, slc3a1, abcc2, neu1, alad, ass1, pc, l2hgdh, opa3, gnmt, lrpprc,
npc2, coq6, LOC579215, bckdha, pnpt1, mgme1, xdh, mocs1, bmp2, gatm, slc35c1, idh2, psat1, fech, acad9,
cln3, gns, cog5, cpt2, taz, lyrm7, mtnr1b, fah, rft1, gusb, auh, aass, stt3b, ethe1, slc35a2,
pdhb, amt, acox1, LOC548617, uqcrb, smpd1, stt3a, sdha, npc1, uqcc2, dlat, slc17a5, gmppa, ngly1, cps1,
tsfm, cyc1, mrpl3, pepd, tat, dpm1, gcsh, ptpn1, cog4, hnf4a, aprt, slc7a9.4, galns, stx16, galk1,
ahcy, phkb, tk2, fars2, dolk, galt, ndufs4, cog1, amacr, pts, mrps16, atp5f1a
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
disease (is_a)