Barraquer–Simons syndrome
Acquired partial lipodystrophy, or Barraquer-Simons syndrome, is characterised by the association of lipoatrophy of the upper part of the body and lipohypertrophy of the thighs
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Barraquer–Simons syndrome
Summary
Barraquer–Simons syndrome is a developmental defect during embryogenesis[1]. It draws 11 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #125 of 308).[2]
Key Facts
- Barraquer–Simons syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Barraquer–Simons syndrome's instance of is recorded as class of disease[4].
- Luis Barraquer Roviralta is named after Barraquer–Simons syndrome[5].
- Arthur Simons is named after Barraquer–Simons syndrome[6].
- Barraquer–Simons syndrome's subclass of is recorded as lipodystrophy[7].
- Barraquer–Simons syndrome's subclass of is recorded as developmental anomaly of metabolic origin[8].
- Barraquer–Simons syndrome's subclass of is recorded as partial lipodystrophy[9].
- Barraquer–Simons syndrome's subclass of is recorded as acquired lipodystrophy[10].
- Barraquer–Simons syndrome's subclass of is recorded as progeroid syndrome[11].
- Barraquer–Simons syndrome's MeSH descriptor ID is recorded as C562448[12].
- Barraquer–Simons syndrome's OMIM ID is recorded as 608709[13].
- Barraquer–Simons syndrome's ICD-9 ID is recorded as 272.6[14].
- Barraquer–Simons syndrome's ICD-10 ID is recorded as E88.1[15].
- Barraquer–Simons syndrome's DiseasesDB is recorded as 9697[16].
- Barraquer–Simons syndrome's National Library of Latvia ID is recorded as 000334377[17].
- Barraquer–Simons syndrome's Orphanet ID is recorded as 79087[18].
- Barraquer–Simons syndrome's NCI Thesaurus ID is recorded as C129723[19].
- Barraquer–Simons syndrome's health specialty is recorded as endocrinology[20].
- Barraquer–Simons syndrome's genetic association is recorded as LMNB2[21].
- Barraquer–Simons syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_79087[22].
- Barraquer–Simons syndrome's UMLS CUI is recorded as C0220989[23].
- Barraquer–Simons syndrome's Medical Dictionary for Regulatory Activities ID is recorded as 10024608[24].
- Barraquer–Simons syndrome's ICD-10-CM is recorded as E88.1[25].
- Barraquer–Simons syndrome's PatientsLikeMe condition ID is recorded as barraquer-simons-syndrome[26].
- Barraquer–Simons syndrome's GARD rare disease ID is recorded as 10509[27].
Why It Matters
Barraquer–Simons syndrome draws 11 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #125 of 308).[2] It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[28] It is known by 11 alternative names across languages and contexts.[29]