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DOID:28 - endocrine system disease
Disease Ontology Definition:A disease of anatomical entity that is located_in endocrine glands which secretes a type of hormone directly into the bloodstream to regulate the body.
Synonyms:
Xenbase Genes : gdf9, foxe1, avp, fgfr3, bmp15, hras, ttr, ar, il6, sox10, spry4, apc, igf2r, fgf8, met, [+]
zfpm2, il17rd, nr2f2, ctla4, hesx1, pdx1, dhh, pax8, smarca4, wnt4, hnf1a, mc2r, akt2, tp53, ptf1a,
fshb, sox3, akt1, ret, otx2, nr5a1, tshb, smad4, ins, nkx2-1, lhb, esr2, fst, slc5a5, foxl2,
amhr2, axin1, ctnnb1, casp8, gh1, nr0b1, nkx2-5, spink1, anos1, lhx3, prokr2, brca1, palld.2, flrt3, inhba,
dicer1, pten, gcm2, kit, lhx4, sh2b3, prok2, clcn2, dcc, ptpn22, cftr, pou1f1, palld, prkar1a, chd7,
tpo, armc5, rnpc3, insr, men1, pdgfrl, axl, sema3e, ntrk1, aip, gc, gnas, bcl10, cdc73, sstr5,
polr3h, minpp1, manf, hs6st1, stk11, sdha, cdh23, pcm1, cyb5a, gnrh1, hsd11b1, cyp11a1, sema3a, figla, usp8,
sdhb, cbx2, sdhc, iyd, fmr1, dusp6, ccdc6, gck, gpr101, tacr3, fezf1, hsd17b3, fshr, lhcgr, psmc3ip,
h6pd, kiss1r, sdhaf2, tshr, pof1b, wdr11, sra1, trim24, crh, pde8b, stag3, nsmf, abcc8, pik3ca, mrps22,
nup107, hadh, ercc6, map3k1, ncoa4, glud1, ifih1, rxfp2, itpr3, srgap1, slc16a1, golga5, rad51d, rad51c, pth,
fgfr1, sox9, trim33, pdgfrl.2, gnrhr, prss1, ctrc, polr3b, spidr, opcml, akr1c2, sdhd, hfm1, akr1c4, kcnj5,
prkaca, mkrn3, ndufa13, thra, smad10, pde11a, kras, duox2, cyp11b2, casr, prss2, thrb, tg, prss1.2, kcnj11,
nras, diaph2, kiss1, btk, brca2, amh, foxp3, aire, ccdc141, serpina6, cdh1, prop1
MONDO:0005151 - endocrine system disorder |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
disease of anatomical entity (is_a)