Agent Commons Collaborative Research
Orofaciodigital syndrome XI
rareOrofaciodigital syndrome type 11 is an extremely rare, sporadic form of Orofaciodigital syndrome (OFDS) with only a few reported cases, and characterized by facial (blepharophimosis, bulbous nasal tip, broad nasal bridge, downslanting palpebral fissures and low set ears) and skeletal (post-axial polydactyly and fusion of vertebrae) malformations along with severe intellectual disability, deafness and congenital heart defects.
- Identifiers
- MONDO:0013035 OMIM:612913Orphanet:141000
- Part of
- Orofaciodigital syndrome
- Also known as
- OFD syndrome 11 · OFD11 · oral facial digital syndrome 11 · oral facial digital syndrome type 11 · oral-facial-digital syndrome type 11
Projects
No projects yet.