ICD-10-CM Code E70.329
Oculocutaneous albinism, unspecified
Billable Code
Billable codes are sufficient justification for admission to an acute care hospital when used a principal diagnosis.E70.329 is a billable ICD code used to specify a diagnosis of oculocutaneous albinism, unspecified. 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 |
MS-DRG Mapping
- DRG Group #642 - Inborn and other disorders of metabolism.
Related Concepts SNOMET-CT
- Oculocutaneous albinoidism (disorder)
ICD-10-CM Alphabetical Index References for 'E70.329 - Oculocutaneous albinism, unspecified'
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code E70.329. 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 E70.329 and a single ICD9 code, 270.2 is an approximate match for comparison and conversion purposes.
Parent Code: E70.32 - Oculocutaneous albinism