Smith-Lemli-Opitz syndrome

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Summary

Literature (0)

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

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: dhcr7

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0010035 - Smith-Lemli-Opitz syndrome

MONDO:0010035 - Smith-Lemli-Opitz syndrome

MIM:

MIM:270400 - SMITH-LEMLI-OPITZ SYNDROME; SLOS

MIM:270400 - SMITH-LEMLI-OPITZ SYNDROME; SLOS

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)