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Human Disease and Mouse Model Detail
Human Disease

Term: Focal Facial Dermal Dysplasia 3, Setleis Type; FFDD3
OMIM ID: 227260

Synonyms Bitemporal Forceps Marks Syndrome; Facial Ectodermal Dysplasia; Focal Facial Dermal Dysplasia, Type II, Formerly; Setleis Syndrome
Associated Genes
 There are currently no human or mouse genes associated with this disease in the MGI database.

Mouse Models
Genotype Ref(s)
Allelic Composition Note Genetic Background
Models with phenotypic similarity to human disease where etiologies involve orthologs.1
Twist2tm1(cre)Dor/Twist2tm1(cre)Dor   involves: 129X1/SvJ * C57BL/6 J:169191

1Human genes are associated with this disease. Mouse model genotypes include mutations in the orthologs of these human genes.
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
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Send questions and comments to User Support. 		last database update
04/03/2013
MGI 5.12 		The Jackson Laboratory