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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:
MONDO:0005151 - endocrine system disease |
Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Xenbase Genes

ctla4, hesx1, pdx1, dhh, pax8, smarca4, wnt4, mc2r, tp53, ptf1a, fshb, sox3, akt1, ret, otx2,
nr5a1, tshb, smad4, nkx2-1, lhb, esr2, fst, foxl2, amhr2, axin1, ctnnb1, casp8, gh1, nr0b1, nkx2-5,
spink1, anos1, lhx3, prokr2, brca1, palld.2, flrt3, inhba, dicer1, pten, gcm2, kit, lhx4, prok2, clcn2,
dcc, cftr, pou1f1, palld, prkar1a, chd7, tpo, armc5, rnpc3, men1, pdgfrl, axl, sema3e, ntrk1, aip,
gc, gnas, bcl10, cdc73, sstr5, polr3h, minpp1, manf, hs6st1, stk11, sdha, pcm1, gnrh1, hsd11b1, cyp11a1,
sema3a, figla, usp8, sdhb, cbx2, sdhc, fmr1, dusp6, ccdc6, tacr3, fezf1, fshr, lhcgr, psmc3ip, h6pd,
kiss1r, sdhaf2, tshr, pof1b, wdr11, sra1, trim24, crh, pde8b, stag3, nsmf, pik3ca, mrps22, nup107, ercc6,
map3k1, ncoa4, ifih1, rxfp2, srgap1, golga5, rad51d, rad51c, pth, fgfr1, sox9, trim33, pdgfrl.2, gnrhr, prss1,
ctrc, polr3b, spidr, opcml, akr1c2, sdhd, hfm1, akr1c4, kcnj5, prkaca, ndufa13, thra, smad4.2, pde11a, kras,
duox2, cyp11b2, casr, prss2, thrb, tg, prss1.2, nras, diaph2, kiss1, btk, brca2, amh, aire, ccdc141,
serpina6, cdh1, prop1
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s):
disease of anatomical entity (is_a)