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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
Echinobase Genes
:
orc1,
cdc6,
cdt1,
orc6
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)