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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 , metabolic disease
Echinobase Genes

ephx2, asah1, etfdh, slc16a1, aga, alg8, gm2a, agk, coq2, asah1, tmem165, pcca, slc2a1, cog7, mccc1,
mpdu1, ears2, cog6, pccb, acadvl, bcs1l, mpi, alg9, gfm1, sucla2, pex1, lmbrd1, gale, tpmt, ppt1,
klf11, 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, bckdk, ctsd, rmnd1, slc25a1, hnf1a,
hpd, acads, LOC583929, 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, pign, gcsh, pigt, 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)