encephalocraniocutaneous lipomatosis
rare neoplastic syndrome characterized by the presence of unilateral lipomas of the cranium, face and neck, and ipsilateral cerebral malformations
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encephalocraniocutaneous lipomatosis
Summary
encephalocraniocutaneous lipomatosis is a hereditary disorder[1]. It draws 25 Wikipedia views per month (hereditary_disorder category, ranking #15 of 25).[2]
Key Facts
- encephalocraniocutaneous lipomatosis's instance of is recorded as hereditary disorder[3].
- encephalocraniocutaneous lipomatosis's instance of is recorded as rare disease[4].
- encephalocraniocutaneous lipomatosis's instance of is recorded as class of disease[5].
- encephalocraniocutaneous lipomatosis is a type of lipomatosis[6].
- encephalocraniocutaneous lipomatosis is a type of subcutaneous tissue disease[7].
- encephalocraniocutaneous lipomatosis is a type of rare genetic subcutaneous tissue disorder[8].
- encephalocraniocutaneous lipomatosis is a type of inherited skin tumor[9].
- encephalocraniocutaneous lipomatosis's symptoms and signs is recorded as Nevus psiloliparus[10].
- encephalocraniocutaneous lipomatosis's ICD-9-CM is recorded as 757.8[11].
- encephalocraniocutaneous lipomatosis's NCI Thesaurus ID is recorded as C4701[12].
- encephalocraniocutaneous lipomatosis's health specialty is recorded as neurology[13].
- encephalocraniocutaneous lipomatosis's genetic association is recorded as FGFR1[14].
- encephalocraniocutaneous lipomatosis's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2396[15].
Why It Matters
encephalocraniocutaneous lipomatosis draws 25 Wikipedia views per month (hereditary_disorder category, ranking #15 of 25).[2]