AutoICD API

BlockL1-LA0

Structural developmental anomalies primarily affecting one body system

Structural developmental anomalies primarily affecting one body system

Classification

ICD-11

Parent Code

20

Child Codes

28

WHO Foundation

View on WHO

Child Codes (28)

BlockL2-LA0

Structural developmental anomalies of the nervous system

BlockL2-LA1

Structural developmental anomalies of the eye, eyelid or lacrimal apparatus

BlockL2-LA2

Structural developmental anomalies of the ear

BlockL2-LA3

Structural developmental anomalies of the face, mouth or teeth

BlockL2-LA6

Structural developmental anomalies of the neck

BlockL2-LA7

Structural developmental anomalies of the respiratory system

BlockL2-LA8

Structural developmental anomalies of the circulatory system

BlockL2-LB0

Structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord

BlockL2-LB1

Structural developmental anomalies of the digestive tract

BlockL2-LB2

Structural developmental anomalies of the liver, biliary tract, pancreas or spleen

BlockL2-LB3

Structural developmental anomalies of the urinary system

BlockL2-LB4

Structural developmental anomalies of the female genital system

BlockL2-LB5

Structural developmental anomalies of the male genital system

BlockL2-LB6

Structural developmental anomalies of the breast

BlockL2-LB7

Structural developmental anomalies of the skeleton

BlockL2-LC0

Structural developmental anomalies of the skin

BlockL2-LC8

Structural developmental anomalies of the adrenal glands

BlockL3-LA4

Clefts of lip, alveolus or palate

BlockL3-LA8

Structural developmental anomaly of heart or great vessels

BlockL3-LB8

Congenital deformities of fingers or toes

BlockL3-LC0

Developmental hamartomata of the epidermis and epidermal appendages

BlockL3-LC1

Developmental anomalies of skin pigmentation

BlockL3-LC2

Hamartomata derived from dermal connective tissue

BlockL3-LC3

Developmental defects of hair or nails

BlockL3-LC5

Developmental anomalies of cutaneous vasculature

BlockL3-LC6

Congenital anomalies of skin development

LD0Y

Other specified structural developmental anomalies primarily affecting one body system

LD0Z

Structural developmental anomalies primarily affecting one body system, unspecified

Frequently Asked Questions
What is the ICD-11 code for structural developmental anomalies primarily affecting one body system?

The ICD-11 code for structural developmental anomalies primarily affecting one body system is BlockL1-LA0. The full clinical description is "Structural developmental anomalies primarily affecting one body system".

What does ICD-11 code BlockL1-LA0 mean?

ICD-11 code BlockL1-LA0 represents "Structural developmental anomalies primarily affecting one body system". It is classified under the ICD-11 classification system.

What is the ICD-10 equivalent of ICD-11 code BlockL1-LA0?

There is no direct ICD-10 mapping available for BlockL1-LA0 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-10. Use the ICD-11 to ICD-10 converter to search for related codes.

What is the difference between ICD-10 and ICD-11?

ICD-11 is the latest revision of the WHO's International Classification of Diseases, succeeding ICD-10. Key differences include: a fully digital-first design, new chapters for sleep-wake disorders, sexual health, and traditional medicine, improved coding for rare diseases, and better integration with electronic health records through extension codes.

What are the subcategories under BlockL1-LA0?

BlockL1-LA0 has 28 child codes, including: BlockL2-LA0 (Structural developmental anomalies of the nervous system), BlockL2-LA1 (Structural developmental anomalies of the eye, eyelid or lacrimal apparatus), BlockL2-LA2 (Structural developmental anomalies of the ear), BlockL2-LA3 (Structural developmental anomalies of the face, mouth or teeth), and 24 more.

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