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Summary Literature (0)
DOID:0060306 - Meier-Gorlin syndrome

Disease Ontology Definition:A syndrome that is characterized by bilateral underdevelopment of the external ear, short stature, absent or underdeveloped patellae and severe prenatal and postnatal growth retardation.

Synonyms: ear-patella-short stature syndrome

Xenbase Genes : orc6, gmnn, cdc6, cdc45, orc1, orc4, cdt1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0016817 - Meier-Gorlin syndrome


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), syndrome (is_a)