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

2025 ICD-10-CM code Q87.81

Alport syndrome, a rare genetic disorder affecting the kidneys, ears, and eyes.

2025 ICD-10-CM code Q87.43

Marfan syndrome with skeletal manifestations.

2025 ICD-10-CM code Q81.9

Epidermolysis bullosa, unspecified; a group of inherited skin disorders causing blistering.

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 Q84.2

This code represents other congenital malformations of hair, including congenital hypertrichosis and persistent lanugo.

2025 ICD-10-CM code Q89.09

Congenital malformations of the spleen; congenital splenomegaly.

2025 ICD-10-CM code Q85

Phakomatoses, not elsewhere classified.

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.

2025 ICD-10-CM code Q86

Congenital malformation syndromes due to known exogenous causes, not elsewhere classified.

2025 ICD-10-CM code Q89.01

Congenital absence of the spleen.

2025 ICD-10-CM code Q81.0

Epidermolysis bullosa simplex, a chronic skin disorder characterized by blister formation on the skin and mucous membranes.

2025 ICD-10-CM code Q87

Other specified congenital malformation syndromes affecting multiple systems.Additional codes should be used to identify all associated manifestations.

2025 ICD-10-CM code Q84

Other congenital malformations of the integument.

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 Q81.2

Epidermolysis bullosa dystrophica is a genetic skin disorder causing blisters and scarring.

2025 ICD-10-CM code Q85.83

Von Hippel-Lindau syndrome, a rare inherited disorder causing tumors and cysts in various body parts.

2025 ICD-10-CM code Q89.7

Multiple congenital malformations, not elsewhere classified.

2025 ICD-10-CM code Q81

Epidermolysis bullosa is a group of inherited skin disorders causing fragile skin and blister formation.

2025 ICD-10-CM code Q87.40

Marfan syndrome, unspecified.Use additional codes to specify associated manifestations.

2025 ICD-10-CM code Q80.8

Other congenital ichthyosis.

2025 ICD-10-CM code Q85.03

Schwannomatosis is a rare genetic disorder characterized by the development of multiple benign schwannomas (tumors on nerves).

2025 ICD-10-CM code Q80.9

Congenital ichthyosis, unspecified.

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