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DOID:0050790 - fibular hypoplasia and complex brachydactyly
Disease Ontology Definition:An autosomal recessive disease that is characterised by severe reduction or absence of the fibula and complex brachydactyly.
Synonyms: Du Pan syndrome,
Echinobase Genes :
MIM:228900 - fibular hypoplasia and complex brachydactyly |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autosomal recessive disease (is_a)