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Coding for Orthognathic Surgery - American Association of Oral and ...

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B. ICD-9-CM codes <strong>for</strong> Syndromes <strong>and</strong> Conditions Requiring<br />

<strong>Orthognathic</strong> <strong>Surgery</strong><br />

Some orthognathic cases may result from syndromes<br />

<strong>and</strong> conditions requiring the surgeon to use the following<br />

codes as primary diagnoses in t<strong>and</strong>em with the<br />

developmental codes listed above (see Section IIIA).<br />

In such cases, the developmental codes will represent<br />

secondary diagnoses.<br />

These syndromes are listed below, followed by a parenthetical<br />

code <strong>and</strong> descriptor.<br />

237.7 Neur<strong>of</strong>ibromatosis/von<br />

Recklinghausen’s disease<br />

(see m<strong>and</strong>ibular asymmetry:<br />

Hyperplasia-524.02, or<br />

Hypoplasia-524.04) (5th digit required)<br />

253.0 Acromegaly (see m<strong>and</strong>ibular<br />

hyperplasia-524.02)<br />

282.4 Thalassemia (see unspecified acquired<br />

de<strong>for</strong>mity <strong>of</strong> head 738.10)<br />

(5th digit required)<br />

346.8 Mobius syndrome (see m<strong>and</strong>ibular<br />

hypoplasia-524.04)<br />

520.5 Amelogenesis imperfecta (see alveolar<br />

maxillary hyperplasia-524.71, <strong>and</strong> also<br />

m<strong>and</strong>ibular hyperplasia-524.02 usually,<br />

both <strong>of</strong> these codes will be required <strong>for</strong><br />

secondary diagnosis <strong>of</strong> amelogenesis<br />

imperfecta)<br />

526.89 Unilateral condylar hyperplasia or<br />

hypoplasia <strong>of</strong> m<strong>and</strong>ible (since this is the<br />

only code <strong>for</strong> the condyle, there is no<br />

secondary code)<br />

733.3 Hyperostosis <strong>of</strong> Skull (includes Stewart-<br />

Morel syndrome <strong>and</strong> Leontiasis ossium)<br />

733.81 Malunion <strong>of</strong> fracture (see the<br />

appropriate developmental diagnosis)<br />

(also use late effect code 905.0)<br />

733.82 Nonunion <strong>of</strong> fracture (see the<br />

appropriate developmental diagnosis)<br />

(also use late effect code 905.0)<br />

754.0 Hemifacial atrophy or hemifacial<br />

hypertrophy (see the appropriate<br />

developmental diagnosis or see<br />

unilateral condyle hyperplasia or<br />

hypoplasia or m<strong>and</strong>ible)<br />

<strong>Coding</strong> Paper<br />

755.55 Apert’s syndrome/<br />

Acrocephalosyndactyly (see maxillary<br />

hypoplasia-524.03)<br />

Pfeiffer syndrome (see maxillary<br />

hypoplasia-524.03, <strong>and</strong> unspecified<br />

acquired de<strong>for</strong>mity <strong>of</strong> head-738.10)<br />

755.59 Cleidocranial Dysplasia/<br />

Cleidocranial Dysotosis (see maxillary<br />

hypoplasia-524.03, <strong>and</strong> also alveolar<br />

maxillary hyperplasia-524.71)<br />

756.0 The following syndromes fall under ICD<br />

9 CM 756.0 [no 5th digit]:<br />

Crouzon’s disease (Crani<strong>of</strong>acial<br />

dysostosis) (see maxillary<br />

hypoplasia-524.03, <strong>and</strong> also unspecified<br />

acquired de<strong>for</strong>mity <strong>of</strong> head-738.10)<br />

Goldenhar syndrome/Hemifacial<br />

Microsomia (see m<strong>and</strong>ibular<br />

hypoplasia-524.04, <strong>and</strong> also<br />

microgenia-524.06)<br />

Hallermann-Streiff syndrome (see<br />

m<strong>and</strong>ibular hypoplasia-524.04, <strong>and</strong> also<br />

microgenia-524.06)<br />

Robin Complex/Pierre-Robin<br />

syndrome/ Robin Anomalad (see<br />

m<strong>and</strong>ibular hypoplasia-524.04, <strong>and</strong> also<br />

microgenia-524.06)<br />

Treacher-Collins syndrome/<br />

M<strong>and</strong>ibul<strong>of</strong>acial Dysostosis (see<br />

zygomatic hypoplasia-738.12,<br />

M<strong>and</strong>ibular Hypoplasia-524.04, <strong>and</strong> also<br />

unilateral condyle hypoplasia-526.89.<br />

Note: Use all secondary codes)<br />

756.4 Achondroplasia (see maxillary<br />

hypoplasia-524.03)<br />

756.51 Osteogenesis Imperfecta (see<br />

m<strong>and</strong>ibular hyperplasia-524.02)<br />

PAGE 3 <strong>Coding</strong> <strong>for</strong> <strong>Orthognathic</strong> <strong>Surgery</strong>

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