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  2. 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]

  3. Necrotizing sialometaplasia - Wikipedia

    en.wikipedia.org/wiki/Necrotizing_sialometaplasia

    Necrotizing sialometaplasia (NS) is a benign, ulcerative lesion, usually located towards the back of the hard palate. It is thought to be caused by ischemic necrosis (death of tissue due to lack of blood supply) of minor salivary glands in response to trauma. Often painless, the condition is self-limiting and should heal in 6–10 weeks.

  4. 2p15-16.1 microdeletion syndrome - Wikipedia

    en.wikipedia.org/wiki/2p15-16.1_microdeletion...

    [1] [2] [3] The shared clinical features include moderate to severe intellectual disability and similar facial features including telecanthus, drooping eyelids, downslanting, short palpebral fissures, a prominent nasal bridge, high palate with long, smooth philtrum and an everted lower lip.

  5. Angina bullosa haemorrhagica - Wikipedia

    en.wikipedia.org/wiki/Angina_bullosa_haemorrhagica

    Angina bullosa haemorrhagica is a condition of the mucous membranes characterized by the sudden appearance of one or more blood blisters within the oral cavity. [1]: 808 The lesions, which may be caused by mild trauma to the mouth tissues such as hot foods, typically rupture quickly and heal without scarring or further discomfort. [2]

  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. Kaufman oculocerebrofacial syndrome - Wikipedia

    en.wikipedia.org/wiki/Kaufman_oculocerebrofacial...

    Kaufman oculocerebrofacial syndrome, also known as blepharophimosis-ptosis-intellectual disability syndrome, is an extremely rare autosomal recessive congenital disorder characterized by severe mental retardation, brachycephaly, upslanting palpebral fissures, eye abnormalities, and highly arched palate.

  8. Blood culture - Wikipedia

    en.wikipedia.org/wiki/Blood_culture

    Blood is normally sterile. [1] The presence of bacteria in the blood is termed bacteremia, and the presence of fungi is called fungemia. [2] Minor damage to the skin [3] or mucous membranes, which can occur in situations like toothbrushing or defecation, [4] [5] can introduce bacteria into the bloodstream, but this bacteremia is normally transient and is rarely detected in cultures because the ...

  9. Oral and maxillofacial pathology - Wikipedia

    en.wikipedia.org/wiki/Oral_and_maxillofacial...

    [8] [9] [10] The most common form is combined cleft lip and palate and it accounts for approximately 50% of cases, whereas isolated cleft lip concerns 20% of the patients. [11] People with cleft lip and palate malformation tend to be less social and report lower self-esteem, anxiety and depression related to their facial malformation.