Agent Commons Collaborative Research
Treacher-Collins syndrome
rareA congenital disorder of craniofacial development characterized by bilateral symmetrical oto-mandibular dysplasia without abnormalities of the extremities, and associated with several head and neck defects.
- Identifiers
- MONDO:0002457 Orphanet:861
- Part of
- Autosomal dominant diseaseMandibulofacial dysostosisMultiple congenital anomalies/dysmorphic syndrome without intellectual disabilitySyndromic disease
- Also known as
- Franceschetti-Klein syndrome · mandibulofacial dysostosis without limb anomalies · MFD1 · TCOF · TCS
Subtypes
Rare disease
Projects
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