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ALL MEDICAL CODES IN CATEGORY Other congenital malformations (Q80-Q89)

2025 ICD-10-CM code Q85.1

Tuberous sclerosis, also known as Bourneville's disease or epiloia, is a genetic disorder characterized by the development of benign tumors in various organs.

2025 ICD-10-CM code Q80.0

Ichthyosis vulgaris is a common, inherited skin disorder characterized by dry, scaly skin.

2025 ICD-10-CM code Q87.19

Other congenital malformation syndromes predominantly associated with short stature.

2025 ICD-10-CM code Q84.6

This code represents other congenital malformations of the nails, including conditions like congenital clubnail and congenital koilonychia.

2025 ICD-10-CM code Q82.2

Congenital cutaneous mastocytosis, encompassing congenital diffuse cutaneous mastocytosis, congenital maculopapular cutaneous mastocytosis, and congenital urticaria pigmentosa.

2025 ICD-10-CM code Q86.2

Dysmorphism due to warfarin exposure during pregnancy.

2025 ICD-10-CM code Q82.3

Incontinentia pigmenti is a rare, X-linked dominant genetic disorder primarily affecting females, characterized by skin lesions following Blaschko's lines, and potentially affecting teeth, hair, nails, eyes, and the central nervous system.

2025 ICD-10-CM code Q83

Congenital malformations of breast

2025 ICD-10-CM code Q87.418

Marfan syndrome with other cardiovascular manifestations.

2025 ICD-10-CM code Q85.81

PTEN hamartoma tumor syndrome (PHTS), also known as PTEN-related Cowden syndrome.This code may also be used for genetic susceptibility to malignant neoplasm (Z15.0-).

2025 ICD-10-CM code Q87.8

Other specified congenital malformation syndromes, not elsewhere classified.

2025 ICD-10-CM code Q80

Congenital ichthyosis.

2025 ICD-10-CM code Q82.4

Ectodermal dysplasia (anhidrotic).

2025 ICD-10-CM code Q81.1

Epidermolysis bullosa letalis, also known as Herlitz-Pearson-type epidermolysis bullosa. A severe, inherited skin disorder characterized by widespread blistering and erosions.

2025 ICD-10-CM code Q82.1

Xeroderma pigmentosum is a rare genetic disorder characterized by extreme sensitivity to ultraviolet (UV) light.

2025 ICD-10-CM code Q82.6

Congenital sacral dimple. This is a minor congenital malformation characterized by a small dimple or pit in the skin at the base of the spine, in the sacral area.

2025 ICD-10-CM code Q84.3

Anonychia. This is a congenital absence of nails.

2025 ICD-10-CM code Q89.1

Congenital malformations of adrenal gland.

2025 ICD-10-CM code Q84.0

Congenital alopecia. Congenital atrichosis.

2025 ICD-10-CM code Q89.8

Other specified congenital malformations. Use additional code(s) to identify all associated manifestations.

2025 ICD-10-CM code Q85.0

Neurofibromatosis (nonmalignant).

2025 ICD-10-CM code Q85.00

Neurofibromatosis, unspecified; a genetic disorder causing tumors to grow along nerves.

2025 ICD-10-CM code Q85.9

Phakomatosis, unspecified. This code is used to classify unspecified phakomatosis, a group of developmental disorders characterized by benign tumors.

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