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DOID:0111591 - congenital heart defects, hamartomas of tongue, and polysyndactyly
Disease Ontology 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.
Synonyms: CHDTHP, Ostravik-Lindemann-Solberg syndrome, heart defect-tongue hamartoma-polysyndactyly syndrome,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee