ICD-10-CM Code E70.321
Tyrosinase positive oculocutaneous albinism
Billable Code
Billable codes are sufficient justification for admission to an acute care hospital when used a principal diagnosis.E70.321 is a billable ICD code used to specify a diagnosis of tyrosinase positive oculocutaneous albinism. A 'billable code' is detailed enough to be used to specify a medical diagnosis.
The ICD code E7032 is used to code Waardenburg syndrome
Waardenburg syndrome (also Waardenburg Shah Syndrome, Waardenburg-Klein syndrome) is a rare genetic disorder most often characterized by varying degrees of deafness, minor defects in structures arising from the neural crest, and pigmentation anomalies.
| Specialty: | Endocrinology |
| MeSH Code: | D014849 |
| ICD 9 Code: | 270.2 |
Coding Notes for E70.321 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. - Albinism II
- Oculocutaneous albinism ty-pos
MS-DRG Mapping
- DRG Group #642 - Inborn and other disorders of metabolism.
ICD-10-CM Alphabetical Index References for 'E70.321 - Tyrosinase positive oculocutaneous albinism'
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code E70.321. Click on any term below to browse the alphabetical index.
Equivalent ICD-9 Code 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 E70.321 and a single ICD9 code, 270.2 is an approximate match for comparison and conversion purposes.
Parent Code: E70.32 - Oculocutaneous albinism