|
DOID:0060342 - acromelic frontonasal dysostosis
Disease Ontology Definition:A dysostosis characterized by cranium bifidum, severe hypertelorism, median cleft lip and palate, nasal bifurcation, brachycephaly, large fontanelle, tibial hemimelia, preaxial polydactyly of the feet and brain malformations.
Synonyms:
Xenbase Genes
:
zswim6
| MONDO:0011359 - acromelic frontonasal dysostosis |
| MIM:603671 - ACROMELIC FRONTONASAL DYSOSTOSIS; AFND |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autosomal dominant disease (is_a),
dysostosis (is_a)