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DOID:16 - integumentary system disease
Disease Ontology Definition:A disease of anatomical entity that is located_in the integumentary system comprising the skin and its appendages.
Synonyms:
Xenbase Genes
:
tgfbr1,
fzd6,
fgfr3,
hras,
atp6v1a,
aqp5,
lrp1,
mfn2,
foxc2,
psen1,
stat1,
tubb,
cdh3,
fgf5,
ncf2,
[+]
pparg, tek, gata1, mmp1, ctnnb1, snai2, smo, socs3, ptch1, gjb3, jup, gsn, itga6, cav1, kitlg,
krt17, rab27a, osmr, lox, dsp, ppp1r3a, kit, smarcad1, tgif1, adar, psenen, gja1, itpr2, lmna, ctsc,
agpat2, aagab, ncf4, adam10, urod, usb1, plin1, mbtps2, fbn1, zmpste24, ncstn, bscl2, cers3, cyba, trpm4,
atp6v0a2, cidec, atp2c1, ap1s3, nhp2, tat, samhd1, cybc1, cybb, ikbkg, pofut1, rpl21, fbln5, gpnmb, cast,
lamb3, lama3, kdsr, card9, tgm5, chst8, lipe, card14, lamc2, ltbp4, sh3bp2, cavin1, recql4, pik3ca, mutyh,
mlph, ncf1, uros, ercc8, pola1, abcb6, nop10, dst, sat1, parn, flcn, myo5a, f12, atp6v1e1, nipal4,
ercc6, st14, atp7a, atp2a2, plcd1, trpv3, sts, tgm1, efemp2, itgb4, ca12, pycr1, npm1, cyld, ptch2,
tinf2, apcdd1, aldh18a1, dkc1, bms1, socs3l, uvssa, liph, cyp4f22, alox12b, snrpe, wrap53, fermt1, aloxe3, traf3ip2,
rtel1, abca12, adgre2, gjb4, rasa1, nras, lpar6, tert, ctc1, pmvk, poglut1, mapre2, plec, il17ra, il17rc,
pnpla1, col17a1, terc, krt9.1, krt9.2, col7a1
| MONDO:0002051 - KIR3DL1 |
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)