About   Help   FAQ
Human Disease and Mouse Model Detail
Human Disease Smith-Lemli-Opitz Syndrome; SLOS
OMIM ID: 270400
Human Phenotype Ontology associations
Synonyms Lethal Acrodysgenital Syndrome; Polydactyly, Sex Reversal, Renal Hypoplasia, and Unilobar Lung; RSH Syndrome; Rutledge Lethal Multiple Congenital Anomaly Syndrome; SLO Syndrome
View all models View ALL (4) mouse models for this human disease.
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     DHCR7* Dhcr7* View 4 models HomoloGene and HGNC
References Disease References using Mouse Models (4)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 6.07
The Jackson Laboratory