E70.39
BillableOther specified albinism
Other specified albinism
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Piebaldism
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Related Codes(4)
Also Known As / Clinical Terms(82)
SNOMED CT
- Chediak-Higashi-like syndrome37548006
- Griscelli syndrome37548006
- Griscelli syndrome with immunodeficiency37548006
- Hypopigmentation-immunodeficiency disease37548006
- Partial albinism with immunodeficiency37548006
- Waardenburg syndrome47434006
- Waardenburg's syndrome47434006
- Sensorineural hearing loss of bilateral ears194424005
- Sensorineural hearing loss of both ears194424005
- Immunodeficiency with major anomalies234631003
- Immunodeficiency associated with multiple organ system abnormalities234641000
- Klein-Waardenberg syndrome237918004
- Klein-Waardenberg's syndrome237918004
- Waardenburg syndrome type 3237918004
- Waardenburg syndrome type III237918004
- Waardenburg syndrome with limb anomalies237918004
- Albinism-deafness syndrome of Tietz403805009
- Ziprkowski-Margolis syndrome403806005
- Phylloid hypomelanosis403807001
- Dead ear700454004
- Profound sensorineural hearing loss700454004
- Piebaldism718122005
- Dystopia canthorum726407000
- Piebald trait with neurologic defects syndrome773984007
- Telfer Sugar Jaeger syndrome773984007
- Profound hearing loss1230412003
- Griscelli syndrome type 11254946006
- Hypopigmentation-immunodeficiency disease type 11254946006
- Griscelli syndrome type 31254947002
- Hypopigmentation-immunodeficiency disease type 31254947002
UMLS
- Other specified albinismC2874233
- PBTC0080024
- PIEBALD TRAITC0080024
- PIEBALDISMC0080024
- Piebald TraitC0080024
- Piebald TraitsC0080024
- Piebald skin depigmentationC0080024
- Piebald traitC0080024
- PiebaldismC0080024
- Piebaldism (disorder)C0080024
- Trait, PiebaldC0080024
- Traits, PiebaldC0080024
- partial albinismC0080024
- piebaldismC0080024
Clinical Terms
- Griscelli syndrome type 3
- Piebaldism (disorder)
- Albinism-deafness syndrome of Tietz
- Piebald trait
- Piebaldism
- Hypopigmentation-immunodeficiency disease
- Piebald trait with neurologic defects syndrome
- Profound sensorineural hearing loss
- Piebald Traits
- Traits, Piebald
- Waardenburg syndrome
- Dead ear
- Telfer Sugar Jaeger syndrome
- Griscelli syndrome type 1
- Partial albinism with immunodeficiency
- Sensorineural hearing loss of bilateral ears
- PBT
- Klein-Waardenberg syndrome
- Piebald skin depigmentation
- Phylloid hypomelanosis
- Dystopia canthorum
- Profound hearing loss
- Waardenburg syndrome type 3
- Waardenburg syndrome with limb anomalies
- Waardenburg's syndrome
- Immunodeficiency with major anomalies
- Sensorineural hearing loss of both ears
- Trait, Piebald
- Griscelli syndrome
- Hypopigmentation-immunodeficiency disease type 1
- Waardenburg syndrome type III
- Hypopigmentation-immunodeficiency disease type 3
- Ziprkowski-Margolis syndrome
- Chediak-Higashi-like syndrome
- partial albinism
- Griscelli syndrome with immunodeficiency
- Klein-Waardenberg's syndrome
- Immunodeficiency associated with multiple organ system abnormalities
Frequently Asked Questions
What is the ICD-10 code for other specified albinism?
The ICD-10-CM code for other specified albinism is E70.39. The full clinical description is "Other specified albinism". E70.39 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E70.39 mean?
ICD-10-CM code E70.39 represents “Other specified albinism”. It is classified under Chapter 4: Endocrine, Nutritional and Metabolic Diseases and is a billable/specific code that can be used on a claim.
Is E70.39 a billable code?
Yes, E70.39 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E70.39 in?
E70.39 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E70.39?
E70.39 has Excludes1 notes indicating codes that cannot be used together with it, including: transitory endocrine and metabolic disorders specific to newborn (P70-P74); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); and 3 more.
What SNOMED CT codes does E70.39 map to?
E70.39 maps to 16 SNOMED CT concepts: 403805009, 37548006, 700454004, 726407000, 1254946006, and 11 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E70.39?
E70.39 is linked to 2 UMLS Concept Unique Identifiers: C2874233, C0080024. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E70.39 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other specified albinism affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of E70.39?
There is no direct ICD-11 mapping available for E70.39 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.
Automate ICD-10 Coding With AI
Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.
Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.