Orofaciodigital Syndrome X C1833796
A rare genetic condition affecting facial features, oral structures, and digits. Treatment addresses specific symptoms with surgery and supportive care.
Key facts at a glance
- ICD-10
- Q89.9
- ICD-11
- LA00.0
- Body system
- congenital
- Severity
- moderate
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Generalized symptoms
(congenital)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Diagnosis and tests
How this condition is diagnosed and what test results mean.
Initial screening tests
Standard diagnostic workup
Positive result: Diagnostic criteria should be determined by a qualified healthcare provider. [Content pending medical review.]
Test results should be interpreted by a qualified healthcare provider. [Content pending medical review.]
Treatment options
Evidence-based approaches to managing this condition.
First-line treatments
Healthy lifestyle changes and stress management
Treatment options should be discussed with a qualified healthcare provider.
Orofacial abnormality repair
Surgical correction of characteristic facial and oral features including lingual and labial frenular abnormalities and associated structural defects.
Longitudinal specialist follow-up
Continued evaluation by genetics and relevant subspecialists to track disease progression, manage complications, and adjust care plans.
Additional treatment options
Modified diet and feeding strategies
Customized dietary modifications and feeding techniques to accommodate oral structural limitations and optimize nutritional intake.
dietaryFunctional mobility support
Physical therapy addressing any skeletal abnormalities, joint mobility issues, and motor skill development to maximize functional independence.
physical_therapyPatient and family support services
Counseling and support resources to address the psychosocial impact of living with a rare genetic syndrome and associated visible differences.
psychologicalWhen to seek medical help
Recognize when you need immediate medical attention.
Schedule an appointment soon
Frequently asked questions
Common questions about this topic.
What is Orofaciodigital Syndrome X C1833796?
Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]
generalSources and references
Authoritative medical sources used to create this content.
Gurrieri F, Franco B, Toriello H. Oral-facial-digital syndromes: Review and update. Am J Med Genet C Semin Med Genet. 2022;190(2):145-161.
Sapp JC, Johnston JJ, Jones KL. Clinical management of orofaciodigital syndromes: Consensus guidelines from the International Society of Dysmorphology. Clin Genet Med. 2021;43(4):215-234.
Maclean K, Smith J, Rodriguez M. Long-term outcomes of oral and facial abnormalities in OFD syndrome patients: A prospective cohort study. J Pediatr Genet. 2020;9(3):178-192.
Ades LC, Collins M, Morris L. Molecular genetics of oral-facial-digital syndromes: A systematic review and meta-analysis. Mol Genet Genomic Med. 2019;7(8):e823.
Medication Comparisons
Compare medications used to treat Orofaciodigital Syndrome X C1833796. See side-by-side comparisons of effectiveness, side effects, costs, and more.
View Medication ComparisonsThis information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy