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DOID:0050691 - branchiooculofacial syndrome
Disease Ontology Definition:A syndrome that is characterized by low birth weight and growth retardation, bilateral branchial clefts.
Synonyms:
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0007235 - branchiooculofacial syndrome |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autosomal dominant disease (is_a),
syndrome (is_a)