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DOID:0050567 - orofacial cleft
Disease Ontology Definition:A physical disorder that is characterized by cleft lip and/or cleft palate that result in feeding, speech and hearing problems caused by failures during development.
Synonyms:
Xenbase Genes
:
bmp4,
msx1,
arhgef38,
sumo1,
tbx22,
mtr,
ric1,
mthfr,
satb2,
specc1l,
cobll1,
ubb
| MONDO:0000358 - blastocyst |
| MIM:119530 - OROFACIAL CLEFT 1; OFC1 |
| MIM:608874 - OROFACIAL CLEFT 5; OFC5 |
| MIM:613705 - OROFACIAL CLEFT 10; OFC10 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
physical disorder (is_a),
syndrome (is_a)