Preferred Name

Treacher-Collins syndrome

ID

http://www.orpha.net/ORDO/Orphanet_861

alternative_term

Mandibulofacial dysostosis without limb anomalies

Franceschetti-Klein syndrome

definition

A rare genetic mandibulofacial dysostosis characterized by bilateral symmetrical oto-mandibular dysplasia including underdeveloped cheekbones (malar hypoplasia), a very small low jaw (micrognathia) and downward-slanting palpebral fissures, coloboma of the lower eyelids, microtia, hearing loss and without abnormalities of the extremities. Intelligence is normal.

definition_citation

Orphanet

expertlink

https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=861

has_age_of_onset

Neonatal

has_inheritance

Autosomal recessive

Autosomal dominant

hasDbXref

OMIM:618939

OMIM:154500

OMIM:248390

ICD-10:Q75.4

MedDRA:10051456

ICD-11:LD2F.16

OMIM:613717

label

Treacher-Collins syndrome

notation

ORPHA:861

part_of

http://www.orpha.net/ORDO/Orphanet_98683

http://www.orpha.net/ORDO/Orphanet_90642

http://www.orpha.net/ORDO/Orphanet_102285

http://www.orpha.net/ORDO/Orphanet_522520

http://www.orpha.net/ORDO/Orphanet_139036

http://www.orpha.net/ORDO/Orphanet_138050

http://www.orpha.net/ORDO/Orphanet_330206

http://www.orpha.net/ORDO/Orphanet_155899

http://www.orpha.net/ORDO/Orphanet_98576

http://www.orpha.net/ORDO/Orphanet_183576

http://www.orpha.net/ORDO/Orphanet_98578

http://www.orpha.net/ORDO/Orphanet_98566

prefixIRI

ORDO:Orphanet_861

prefLabel

Treacher-Collins syndrome

present_in

Europe AND has_point_prevalence_range : 1-9 / 100 000

Japan AND has_birth_prevalence_average_value : 6.9 AND has_birth_prevalence_range : 1-9 / 100 000

Japan AND has_point_prevalence_range : 1-9 / 100 000

France AND has_point_prevalence_range : 1-9 / 1 000 000

France AND has_birth_prevalence_average_value : 0.63 AND has_birth_prevalence_range : 1-9 / 1 000 000

Europe AND has_birth_prevalence_average_value : 2.0 AND has_birth_prevalence_range : 1-9 / 100 000

treeView

http://www.orpha.net/ORDO/Orphanet_98683

http://www.orpha.net/ORDO/Orphanet_90642

http://www.orpha.net/ORDO/Orphanet_102285

http://www.orpha.net/ORDO/Orphanet_522520

http://www.orpha.net/ORDO/Orphanet_139036

http://www.orpha.net/ORDO/Orphanet_138050

http://www.orpha.net/ORDO/Orphanet_330206

http://www.orpha.net/ORDO/Orphanet_155899

http://www.orpha.net/ORDO/Orphanet_98576

http://www.orpha.net/ORDO/Orphanet_183576

http://www.orpha.net/ORDO/Orphanet_98578

http://www.orpha.net/ORDO/Orphanet_98566

subClassOf

http://www.orpha.net/ORDO/Orphanet_377789

http://www.orpha.net/ORDO/Orphanet_557493

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