About   Help   FAQ
Disease Ontology Browser
congenital heart defects, hamartomas of tongue, and polysyndactyly (DOID:0111591)
Alliance: disease page
Synonyms: CHDTHP; heart defect-tongue hamartoma-polysyndactyly syndrome; Ostravik-Lindemann-Solberg syndrome
Alt IDs: OMIM:217085, MESH:C535849, ORDO:1338, UMLS_CUI:C2931046
Definition: A syndrome characterized by congenital heart defects, hamartomas of tongue, and polysyndactyly that has_material_basis_in homozygous or compound heterozygous mutation in the WDPCP gene on chromosome 2p15.


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
11/12/2024
MGI 6.24
The Jackson Laboratory