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DOID:8943 - lattice corneal dystrophy
Disease Ontology Definition:n_a
Synonyms: familial amyloid neuropathy, Finnish type,
Xenbase Genes :
MONDO:0004686 - lattice corneal dystrophy |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
epithelial-stromal TGFBI dystrophy (is_a)