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DOID:9631 - Pelger-Huet anomaly
Disease Ontology Definition:n_a
Synonyms:
Echinobase Genes :
MIM:169400 - pelger-huet anomaly; pha |
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)