H47.619
BillableCortical blindness, unspecified side of brain
Cortical blindness, unspecified side of brain
Coding Notes
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Excludes 2
Conditions not included here, but the patient may have both
- •certain conditions originating in the perinatal periodP04-P96
- •certain infectious and parasitic diseasesA00-B99
- •complications of pregnancy, childbirth and the puerperiumO9A)O00
- •congenital malformations, deformations, and chromosomal abnormalitiesQ00-Q99
- •diabetes mellitus related eye conditions, , ,E09.3, E10.3, E11.3, E13.3
- •endocrine, nutritional and metabolic diseasesE00-E88
- •injury (trauma) of eye and orbitS05
- •injury, poisoning and certain other consequences of external causesS00-T88
- •neoplasmsC00-D49
- •symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classifiedR00-R94
- •syphilis related eye disorders, , ,A50.01, A50.3, A51.43, A52.71
Code Also
A second code may be required; sequencing depends on circumstances
- underlying condition
Related Codes(2)
Also Known As / Clinical Terms(21)
SNOMED CT
- Cortical blindness68574006
- Cortical visual impairment413924001
- Cortical blindness, intellectual disability, polydactyly syndrome732251003
- Early-onset epileptic encephalopathy, cortical blindness, intellectual disability, facial dysmorphism syndrome773548008
- Epilepsy, cortical blindness, intellectual disability, facial dysmorphism syndrome773548008
- Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome1172900005
- Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome with combined immunodeficiency due to diaphanous related formin 1 mutation1354858008
- Progressive microcephaly, seizures, cortical blindness, developmental delay with combined immunodeficiency due to DIAPH1 deficiency1354858008
- Progressive microcephaly, seizures, cortical blindness, developmental delay with combined immunodeficiency due to DIAPH1 mutation1354858008
- SCBMS (seizures, cortical blindness, microcephaly syndrome) with combined immunodeficiency due to DIAPH1 mutation1354858008
Clinical Terms
- Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome with combined immunodeficiency due to diaphanous related formin 1 mutation
- Progressive microcephaly, seizures, cortical blindness, developmental delay with combined immunodeficiency due to DIAPH1 deficiency
- Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome
- SCBMS (seizures, cortical blindness, microcephaly syndrome) with combined immunodeficiency due to DIAPH1 mutation
- Cortical blindness, intellectual disability, polydactyly syndrome
- Early-onset epileptic encephalopathy, cortical blindness, intellectual disability, facial dysmorphism syndrome
- Epilepsy, cortical blindness, intellectual disability, facial dysmorphism syndrome
- Progressive microcephaly, seizures, cortical blindness, developmental delay with combined immunodeficiency due to DIAPH1 mutation
- Cortical visual impairment
- Cortical blindness
Frequently Asked Questions
What is the ICD-10 code for cortical blindness, unspecified side of brain?
The ICD-10-CM code for cortical blindness, unspecified side of brain is H47.619. The full clinical description is "Cortical blindness, unspecified side of brain". H47.619 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code H47.619 mean?
ICD-10-CM code H47.619 represents “Cortical blindness, unspecified side of brain”. It is classified under Chapter 7: Diseases of the Eye and Adnexa and is a billable/specific code that can be used on a claim.
Is H47.619 a billable code?
Yes, H47.619 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is H47.619 in?
H47.619 is in Chapter 7: Diseases of the Eye and Adnexa (codes H00-H59).
What codes cannot be used with H47.619?
H47.619 has Excludes1 notes indicating codes that cannot be used together with it, including: injury to visual cortex S04.04-.
What SNOMED CT codes does H47.619 map to?
H47.619 maps to 6 SNOMED CT concepts: 68574006, 732251003, 413924001, 773548008, 1172900005, and 1 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for H47.619?
H47.619 is linked to 1 UMLS Concept Unique Identifier: C2881269. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does H47.619 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like cortical blindness, unspecified side of brain 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 H47.619?
There is no direct ICD-11 mapping available for H47.619 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.