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Summary Literature (2)
DOID:14692 - Smith-Lemli-Opitz syndrome


Disease Ontology Definition:n_a

Synonyms: Rutledge lethal multiple congenital anomaly syndrome, Smith-Opitz-Inborn syndrome

Referenced OMIM:
OMIM:270400 - SMITH-LEMLI-OPITZ SYNDROME; SLOS

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : dhcr7

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): lipid metabolism disorder (is_a)


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Version: 4.14.0
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