ICD9 Online Home

Free online searchable
2009 ICD-9-CM

Search for  

Diseases and Injuries
>> Tabular Index
>> Alphabetic Index

Procedures
>> Tabular Index
>> Alphabetic Index

Appendices
>> Drugs / Chemicals
>> External Causes

Other Resources
>> HCPCS Alpha
>> Medical Dictionary
>> Drug Directory


Tips
Contribute





Mandibulofacial Dysostosis

Treacher Collins Syndrome | Collins Syndrome, Treacher | Dysostoses, Mandibulofacial | Dysostosis, Mandibulofacial | Mandibulofacial Dysostoses | Syndrome, Treacher Collins

A hereditary disorder occurring in two forms: the complete form (Franceschetti's syndrome) is characterized by antimongoloid slant of the palpebral fissures, coloboma of the lower lid, micrognathia and hypoplasia of the zygomatic arches, and microtia. It is transmitted as an autosomal trait. The incomplete form (Treacher Collins syndrome) is characterized by the same anomalies in less pronounced degree. It occurs sporadically, but an autosomal dominant mode of transmission is suspected. (Dorland, 27th ed)

The National Library of Medicine (terms and conditions)
 
Google
 
Web icd9cm.chrisendres.com