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bn:00250408n
Noun Concept
Categories: Hearing loss with craniofacial syndromes, Genodermatoses, Congenital disorders of musculoskeletal system, Autosomal dominant disorders, Rare diseases
EN
Treacher Collins syndrome  (Mandibulofacial dysostosis) or (Franceschetti syndrome)  Bulofacial dysostosis  Familial Treacher-Collins syndrome  Familial Treacher Collins syndrome
EN
Treacher Collins syndrome is a genetic disorder characterized by deformities of the ears, eyes, cheekbones, and chin. Wikipedia
Definitions
Relations
Sources
EN
Treacher Collins syndrome is a genetic disorder characterized by deformities of the ears, eyes, cheekbones, and chin. Wikipedia
A rare genetic disorder characterised by craniofacial deformities. Wikipedia Disambiguation
Human disease Wikidata
IS A
rare disease
syndrome
First arch syndrome
GENETIC ASSOCIATION
POLR1D
POLR1C
TCOF1
HEALTH SPECIALTY
medical genetics
NAMED AFTER
Edward Treacher Collins
Wikipedia
EN
Treacher Collins syndrome
Wikidata
EN
Treacher Collins syndrome
Wikipedia Redirections
EN
Bulofacial dysostosis, Familial Treacher-Collins syndrome, Familial Treacher Collins syndrome, Familial Treacher–Collins syndrome, Franceschetti-Zwahlen-Klein syndrome, Franceschetti-Zwalen-Klein syndrome, Franceschetti–Zwahlen–Klein syndrome, Juliana Wetmore, Julianna Wetmore, Lancaster's, Lancaster's Disease, Lancaster Disease, MFD1, Treacher-Collins Syndrome, Treacher collin syndrome, Treacher Collins-Franceschetti syndrome, Treacher Collins Syndrome, Treacher collins syndrome, Treacher Collins syndrome protein, Treacher Collins–Franceschetti syndrome, Treachers Collins Syndrome, Treacher–Collins syndrome
Wikidata Alias
EN
Franceschetti-Klein syndrome, Franceschetti syndrome, mandibulofacial dysostosis, Mandibulofacial dysostosis without limb anomalies, (Mandibulofacial dysostosis) or (Franceschetti syndrome)

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