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DOID:14291 - LEOPARD syndrome
Disease Ontology Definition:n_a
Synonyms: Capute-Rimoin-Konigsmark-Esterly-Richardson syndrome, Cardiocutaneous syndrome, Generalized lentiginosis (disorder), Gorlin syndrome II, LEOPARD syndrome, Lentiginosis profusa syndrome, Moynahan syndrome, Multiple lentigines syndrome (disorder), Progressive cardiomyopathic lentiginosis,
Echinobase Genes :
MIM:151100 - leopard syndrome 1 |
MIM:611554 - leopard syndrome 2 |
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)