|
DOID:14692 - Smith-Lemli-Opitz syndrome
Disease Ontology Definition:n_a
Synonyms: Rutledge lethal multiple congenital anomaly syndrome, Smith-Opitz-Inborn syndrome,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
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)