Conditions / Syndrome
orofacial cleft 13
info · Syndrome
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.
Signs and symptoms
- Cleft soft palate
- Malar flattening
- Retrognathia
- Micrognathia
- Oligodontia