ICD-10-CM Code Q82.8
Other specified congenital malformations of skin
Billable Code
Billable codes are sufficient justification for admission to an acute care hospital when used a principal diagnosis.POA Exempt Code
The Center for Medicare & Medicaid Services (CMS) requires medical coders to indicate whether or not a condition was present at the time of admission, in order to properly assign MS-DRG codes. This "Present On Admission" (POA) indicator is recorded on CMS form 4010A.Q82.8 is a billable ICD code used to specify a diagnosis of other specified congenital malformations of skin. A 'billable code' is detailed enough to be used to specify a medical diagnosis.
POA Indicators on CMS form 4010A are as follows:
| Indicator | Meaning | CMS Will Pay CC/MCC DRG Costs |
|---|---|---|
| Y | Diagnosis was present at time of inpatient admission | Yes |
| N | Diagnosis was not present at time of inpatient admission | No |
| U | Documentation insufficient to determine if the condition was present at the time of inpatient admission. | No |
| W | Clinically undetermined. Provider unable to clinically determine whether the condition was present at the time of inpatient admission. | Yes |
| 1 | Exempt from POA reporting | No |
The ICD code Q828 is used to code Schöpf-Schulz-Passarge syndrome
Schöpf–Schulz–Passarge syndrome (also known as "Eyelid cysts, palmoplantar keratoderma, hypodontia, and hypotrichosis") is an autosomal recessive condition with diffuse symmetric palmoplantar keratoderma, with the palmoplantar keratoderma and fragility of the nails beginning around age 12.:513
| Specialty: | Medical Genetics |
| MeSH Codes: | , D007644, C536164, D016506, D019871, , , , , , , D005489, , D003483, D003483 |
| ICD 9 Codes: | , , , 757.39, 757.39, , 701.1, 757.39, , , , 759.89, , 701.8, 756.83 |
Coding Notes for Q82.8 Info for medical coders on how to properly use this ICD-10 code
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Inclusion Terms:
Inclusion Terms
Inclusion Terms are a list of concepts for which a specific code is used. The list of Inclusion Terms is useful for determining the correct code in some cases, but the list is not necessarily exhaustive. - Abnormal palmar creases
- Accessory skin tags
- Benign familial pemphigus [Hailey-Hailey]
- Congenital poikiloderma
- Cutis laxa (hyperelastica)
- Dermatoglyphic anomalies
- Inherited keratosis palmaris et plantaris
- Keratosis follicularis [Darier-White]
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Code Type-1 Excludes:
Type-1 Excludes
Type-1 Excludes mean the conditions excluded are mutually exclusive and should never be coded together. Excludes 1 means "do not code here." - Ehlers-Danlos syndrome - instead, use code Q79.6
MS-DRG Mapping
- DRG Group #606-607 - Minor skin disorders with MCC.
- DRG Group #606-607 - Minor skin disorders without MCC.
- DRG Group #795 - Normal newborn.
Related Concepts SNOMET-CT
- Cutis laxa with osteodystrophy (disorder)
- Multiple progressive hemangiomata (disorder)
- Zosteriform lentiginosis (disorder)
ICD-10-CM Alphabetical Index References for 'Q82.8 - Other specified congenital malformations of skin'
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code Q82.8. Click on any term below to browse the alphabetical index.
Equivalent ICD-9 Codes GENERAL EQUIVALENCE MAPPINGS (GEM)
This is the official approximate match mapping between ICD9 and ICD10, as provided by the General Equivalency mapping crosswalk. This means that while there is no exact mapping between this ICD10 code Q82.8 and a single ICD9 code, 757.39 is an approximate match for comparison and conversion purposes.
Parent Code: Q82 - Other congenital malformations of skin