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

26

WHO Foundation

View on WHO

Child Codes (26)

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

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 26 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 22 more.

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