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DOID:0060261 - congenital ptosis
Disease Ontology Definition:A ptosis characterized by eyelid drop present at birth.
Synonyms:
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0008340 - ptosis, hereditary congenital, 1 |
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),
ptosis (is_a)