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ALL MEDICAL CODES IN CATEGORY Other congenital malformations

2025 ICD-10-CM code Q87.11

Prader-Willi syndrome.

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 Q89

Other congenital malformations, not elsewhere classified.

2025 ICD-10-CM code Q87.410

Marfan syndrome with aortic dilation.

2025 ICD-10-CM code Q87.2

Congenital malformation syndromes predominantly involving limbs.

2025 ICD-10-CM code Q89.9

Congenital malformation, unspecified.

2025 ICD-10-CM code Q87.3

Congenital malformation syndromes involving early overgrowth.

2025 ICD-10-CM code Q87.418

Marfan syndrome with other cardiovascular manifestations.

2025 ICD-10-CM code Q83.9

Congenital malformation of breast, unspecified.

2025 ICD-10-CM code Q83.8

This code signifies other congenital malformations of the breast, encompassing anomalies not otherwise specified in the Q83 category.

2025 ICD-10-CM code Q87.5

Other congenital malformation syndromes with other skeletal changes.

2025 ICD-10-CM code Q80.1

X-linked ichthyosis.

2025 ICD-10-CM code Q89.7

Multiple congenital malformations, not elsewhere classified.

2025 ICD-10-CM code Q87.40

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

2025 ICD-10-CM code Q86.0

Fetal alcohol syndrome (dysmorphic).

2025 ICD-10-CM code Q83.0

Congenital absence of breast with absent nipple.

2025 ICD-10-CM code Q89.3

Situs inversus is a congenital condition in which the major visceral organs are reversed or mirrored from their normal positions.

2025 ICD-10-CM code Q87.82

Arterial tortuosity syndrome.

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 Q85.09

This code signifies other neurofibromatosis, a group of genetic disorders causing tumors to grow along nerves.

2025 ICD-10-CM code Q89.2

Congenital malformations of other endocrine glands, including the parathyroid or thyroid gland, persistent thyroglossal duct, or thyroglossal cyst.

2025 ICD-10-CM code Q89.4

This code represents a condition where two fetuses are physically joined together at birth.

2025 ICD-10-CM code Q87.41

Marfan syndrome with cardiovascular manifestations.

2025 ICD-10-CM code Q89.1

Congenital malformations of adrenal gland.

2025 ICD-10-CM code Q85.82

Other Cowden syndrome.

2025 ICD-10-CM code Q87.0

Congenital malformation syndromes predominantly affecting facial appearance.

2025 ICD-10-CM code Q83.1

Accessory breast. Supernumerary breast.

2025 ICD-10-CM code Q89.0

Congenital absence and malformations of spleen.

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 Q89.01

Congenital absence of the spleen.

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 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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