Cleft lip or cleft palate: Difference between revisions
No edit summary |
Ttenbergen (talk | contribs) m adding {{Data Integrity Check List}} |
||
(8 intermediate revisions by 3 users not shown) | |||
Line 1: | Line 1: | ||
{{ICD10 transition status | {{ICD10 transition status | ||
| OldDxArticle = | | OldDxArticle = | ||
| CurrentStatus = | | CurrentStatus =reconciled | ||
| InitialEditorAssigned = | | InitialEditorAssigned = not assigned | ||
}} | }} | ||
{{ICD10 dx | {{ICD10 dx | ||
Line 13: | Line 13: | ||
== Additional Info == | == Additional Info == | ||
https://en.wikipedia.org/wiki/Cleft_lip_and_cleft_palate | https://en.wikipedia.org/wiki/Cleft_lip_and_cleft_palate | ||
When a patient presents solely for management of a specific manifestation of a congenital anomaly syndrome, assign a code for the manifestation as the main problem. | |||
• Assign an additional code to describe the syndrome. | |||
Example: | |||
A young male patient with Goldenhar syndrome and cleft palate is admitted for a revision of the cleft palate repair. | |||
Cleft palate, unspecified | |||
Congenital malformation syndromes predominantly affecting facial appearance there is a specific code to identify the Goldenhar syndrome. the cleft palate is the condition described as the reason for the patient’s stay in hospital | |||
*Syndromes/The Van der Woude Syndrome/ Siderius X-linked mental retardation/Stickler's Syndrome/Loeys-Dietz syndrome/Hardikar syndrome/Cleft lip/palate may be present in many different chromosome disorders including Patau Syndrome (trisomy 13)/Malpuech facial clefting syndrome/ | |||
Hearing loss with craniofacial syndromes/Popliteal pterygium syndrome/Treacher Collins Syndrome/ | |||
== Alternate ICD10s to consider coding instead or in addition == | == Alternate ICD10s to consider coding instead or in addition == | ||
*[[Chromosomal abnormality, NOS ]] | *[[Chromosomal abnormality, NOS ]] | ||
*[[Face and/or neck, congenital malformation]] | |||
== Candidate [[Combined ICD10 codes]] == | == Candidate [[Combined ICD10 codes]] == | ||
== Related CCI Codes == | == Related CCI Codes == | ||
{{Data Integrity Check List}} | |||
== Related Articles == | == Related Articles == | ||
{{Related Articles}} | {{Related Articles}} | ||
{{ICD10 footer}} | {{ICD10 footer}} | ||
{{EndPlaceHolder}} | {{EndPlaceHolder}} |
Latest revision as of 23:35, 2018 November 17
ICD10 Diagnosis | |
Dx: | Cleft lip or cleft palate |
ICD10 code: | Q37 |
Pre-ICD10 counterpart: | none assigned |
Charlson/ALERT Scale: | none |
APACHE Como Component: | none |
APACHE Acute Component: | none |
Start Date: | |
Stop Date: | |
External ICD10 Documentation |
This diagnosis is a part of ICD10 collection.
Additional Info
https://en.wikipedia.org/wiki/Cleft_lip_and_cleft_palate
When a patient presents solely for management of a specific manifestation of a congenital anomaly syndrome, assign a code for the manifestation as the main problem. • Assign an additional code to describe the syndrome.
Example:
A young male patient with Goldenhar syndrome and cleft palate is admitted for a revision of the cleft palate repair. Cleft palate, unspecified Congenital malformation syndromes predominantly affecting facial appearance there is a specific code to identify the Goldenhar syndrome. the cleft palate is the condition described as the reason for the patient’s stay in hospital
- Syndromes/The Van der Woude Syndrome/ Siderius X-linked mental retardation/Stickler's Syndrome/Loeys-Dietz syndrome/Hardikar syndrome/Cleft lip/palate may be present in many different chromosome disorders including Patau Syndrome (trisomy 13)/Malpuech facial clefting syndrome/
Hearing loss with craniofacial syndromes/Popliteal pterygium syndrome/Treacher Collins Syndrome/
Alternate ICD10s to consider coding instead or in addition
Candidate Combined ICD10 codes
Related CCI Codes
Data Integrity Checks (automatic list)
none found
Related Articles
Show all ICD10 Subcategories