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Illness finder is a diagnostic medicine tool for educational purpose that looks up your patients' health conditions or symptoms and diagnosis and find diseases or illnesses based on chosen gender, age, risk factors, illness, signs, symptoms and prevalence. Illnessfinder is inspired by Evidence based medicine (EMB) and healthcare that aims to apply the best (most reliable) knowledge that is available at decision time. Illnessfinder aims to free up time for the therapeutic dialogue and ensure quality at the evidence based practice, uniting proven medical findings and clinical evidence with systematised data technology.
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| Pachyonychia Congenita | Legal notice |
Other terms
Congenita, Pachyonychia,Pachyonychia Congenita, Type 2,Pachyonychia Congenita, Jackson-Lawler Type,Pachyonychia Congenita, Jackson Lawler Type,Type 2 Pachyonychia Congenita,Jackson-Lawler Type Pachyonychia Congenita,Jackson Lawler Type Pachyonychia Congenita,Steatocystoma Multiplex,Multiplex, Steatocystoma,Multiplices, Steatocystoma,Steatocystoma Multiplices,Pachyonychia Congenita, Type 1,Pachyonychia Congenita Type 1,Pachyonychia Congenita, Jadassohn-Lewandowsky Type,Pachyonychia Congenita, Jadassohn Lewandowsky Type,Type 1 Pachyonychia Congenita,Jadassohn-Lewandowsky Syndrome,Jadassohn Lewandowsky Syndrome,Pachyonychia Congenita Tarda, Type 1
Description
Pachyonychia Congenita: A group of inherited ectodermal dysplasias whose most prominent clinical feature is hypertrophic nail dystrophy resulting in PACHYONYCHIA. Several specific subtypes of pachyonychia congenita have been associated with mutations in genes that encode KERATINS.
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Legal notice
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The version of the data is 2010 MeSH. Last reviewed April 26, 2010. No modification has been made in the content of the file.
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