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DOID:0060306 - Meier-Gorlin syndrome
Disease Ontology Definition:An autosomal recessive disorder characterized by severe intrauterine and postnatal growth retardation, microcephaly, bilateral microtia and hypoplastic patellae.
Synonyms: ear-patella-short stature syndrome,
Echinobase Genes
:
orc1,
cdc6,
cdt1,
orc6
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autosomal recessive disease (is_a)