Smith-Lemli-Opitz syndrome Disease Ontology Browser

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Disease Ontology Browser

Smith-Lemli-Opitz syndrome (DOID:14692)
Alliance: disease page
Synonyms: Rutledge lethal multiple congenital anomaly syndrome; Smith-Opitz-Inborn syndrome
Alt IDs: OMIM:270400, DOID:4366, ICD10CM:E78.72, MESH:D019082, NCI:C85071, UMLS_CUI:C0175694

Disease References using Mouse Models (5)

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/16/2024 MGI 6.23

Allelic Composition	Genetic Background	Reference	Phenotypes
Dhcr7tm1Fdp/Dhcr7tm1Fdp	involves: 129S4/SvJae	J:68084, J:165301	View
Dhcr7tm2Fdp/Dhcr7tm2Fdp	involves: 129S4/SvJae	J:106758	View
Dhcr7tm1Gst/Dhcr7tm1Gst	involves: 129P2/OlaHsd	J:71611	View
Dhcr7tm1Fdp/Dhcr7tm2Fdp	involves: 129S4/SvJae	J:106758	View
Dhcr7tm1.1Sbpa/Dhcr7tm1.1Sbpa Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+	B6.Cg-Dhcr7^tm1.1Sbpa Speer6-ps1^{Tg(Alb-cre)21Mgn}	J:303316	View