| Term Name: | orofacial cleft 13 |
|---|---|
| Synonyms: | |
| Definition: | An orofacial cleft characterized by autosomal dominant inheritance that has_material_basis_in variation in chromosome region 1p33 associated with enrichment of the T allele of SNP rs3827730. |
| Ontology: | Human Disease [DOID:0080406] ( DOID:0080406 ) |