|
DOID:9521 - Laron syndrome
Disease Ontology Definition:n_a
Synonyms: Laron-type isolated somatotropin defect (disorder),
Echinobase Genes :
MIM:262500 - laron syndrome |
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)