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  2. ICD-10-CM - Wikipedia

    en.wikipedia.org/wiki/ICD-10-CM

    The ICD-10 Clinical Modification (ICD-10-CM) is a set of diagnosis codes used in the United States of America. [1] It was developed by a component of the U.S. Department of Health and Human services, [ 2 ] as an adaption of the ICD-10 with authorization from the World Health Organization .

  3. Dermatographic urticaria - Wikipedia

    en.wikipedia.org/wiki/Dermatographic_urticaria

    Dermatographic urticaria is sometimes called "skin writing", as it is possible to mark deliberate patterns onto the skin. The condition manifests as an allergic-like reaction, causing a warm red wheal to appear on the skin.

  4. 7p22.1 microduplication syndrome - Wikipedia

    en.wikipedia.org/wiki/7p22.1_microduplication...

    This condition (as the name implies) is caused by a 430 kB duplication of the p22.1 region of chromosome 7. [3] This mutation is autosomal recessive , meaning that a baby would need 1 copy of a mutated gene from both parents in order to show symptoms of the disorder.

  5. ICD coding for rare diseases - Wikipedia

    en.wikipedia.org/wiki/ICD_coding_for_rare_diseases

    Europe and other parts of the world use the ICD-10. The root codes for ICD-10 and ICD-10-CM are the same, making it helpful for locating codes for general body systems and disease processes. [2] [3] In ICD-11 the search and coding of any disease, including rare ones is done via the ICD-11 website. [4]

  6. ICD-10 - Wikipedia

    en.wikipedia.org/wiki/ICD-10

    ICD-10 is the 10th revision of the International Classification of Diseases (ICD), a medical classification list by the World Health Organization (WHO). It contains codes for diseases, signs and symptoms, abnormal findings, complaints, social circumstances, and external causes of injury or diseases. [1]

  7. Pfeiffer syndrome - Wikipedia

    en.wikipedia.org/wiki/Pfeiffer_syndrome

    Pfeiffer syndrome is a rare genetic disorder, characterized by the premature fusion of certain bones of the skull (craniosynostosis), which affects the shape of the head and face. The syndrome includes abnormalities of the hands and feet, such as wide and deviated thumbs and big toes.

  8. Frontonasal dysplasia - Wikipedia

    en.wikipedia.org/wiki/Frontonasal_dysplasia

    Frontonasal dysplasia (FND) is a congenital malformation of the midface. [1] For the diagnosis of FND, a patient should present at least two of the following characteristics: hypertelorism (an increased distance between the eyes), a wide nasal root, vertical midline cleft of the nose and/or upper lip, cleft of the wings of the nose, malformed nasal tip, encephalocele (an opening of the skull ...

  9. Inflammatory linear verrucous epidermal nevus - Wikipedia

    en.wikipedia.org/wiki/Inflammatory_Linear...

    Inflammatory Linear Verrucous Epidermal Nevus is a rare disease of the skin that presents as multiple, discrete, red papules that tend to coalesce into linear plaques that follow the Lines of Blaschko.