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DOID:14692 - Smith-Lemli-Opitz syndrome
Disease Ontology Definition:n_a
Synonyms: Rutledge lethal multiple congenital anomaly syndrome, Smith-Opitz-Inborn syndrome,
Xenbase Genes : dhcr7
MONDO:0010035 - Smith-Lemli-Opitz syndrome |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
lipid metabolism disorder (is_a)