lipoid proteinosis
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lipoid proteinosis
Summary
lipoid proteinosis is a developmental defect during embryogenesis[1]. It has Wikipedia articles in 13 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- lipoid proteinosis's instance of is recorded as developmental defect during embryogenesis[3].
- lipoid proteinosis's instance of is recorded as rare disease[4].
- lipoid proteinosis's instance of is recorded as class of disease[5].
- Erich Urbach is named after lipoid proteinosis[6].
- Camillo Wiethe is named after lipoid proteinosis[7].
- lipoid proteinosis is a type of lipid metabolism disorder[8].
- lipoid proteinosis is a type of other genetic dermis disorder[9].
- lipoid proteinosis is a type of malformation syndrome with skin/mucosae involvement[10].
- lipoid proteinosis is a type of rare dyslipidemia[11].
- lipoid proteinosis is a type of developmental anomaly of metabolic origin[12].
- lipoid proteinosis is a type of other dermis disorder[13].
- lipoid proteinosis is a type of hoarseness[14].
- lipoid proteinosis is a type of disease[15].
- lipoid proteinosis's Commons category is recorded as Urbach–Wiethe disease[16].
- lipoid proteinosis's ICD-9-CM is recorded as 272.8[17].
- lipoid proteinosis's NCI Thesaurus ID is recorded as C84829[18].
- lipoid proteinosis's health specialty is recorded as endocrinology[19].
- lipoid proteinosis's genetic association is recorded as ECM1[20].
- lipoid proteinosis's exact match is recorded as http://purl.obolibrary.org/obo/DOID_14498[21].
- lipoid proteinosis's exact match is recorded as http://identifiers.org/doid/DOID:14498[22].
- lipoid proteinosis's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_530[23].
- lipoid proteinosis's on focus list of Wikimedia project is recorded as WikiProject Medicine[24].
Why It Matters
lipoid proteinosis has Wikipedia articles in 13 language editions, a strong signal of global cultural recognition.[2] It is known by 11 alternative names across languages and contexts.[25]