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The way concept relations are shown:
Lipodystrophy, Familial Partial
Hierarchy: | ∟ ∟ ∟ ∟ ∟ Lipodystrophy, Familial Partial 2 coordinate concepts∟ ∟ ∟ ∟ ∟ Lipodystrophy, Familial Partial 2 coordinate concepts∟ ∟ ∟ ∟ ∟ Lipodystrophy, Familial Partial 2 coordinate conceptsX |
Broader terms: | ∟ ∟ ∟ ∟ ∟ Lipodystrophy, Familial Partial ∟ ∟ ∟ ∟ ∟ Lipodystrophy, Familial Partial ∟ ∟ ∟ ∟ ∟ Lipodystrophy, Familial Partial |
History note: | Lipodystrophy (1975-2006)X |
historyNote*: | 2007; use DIABETES MELLITUS, LIPOATROPHIC 2005-2006
X |
publicMeSHNote*: | 2007; see DIABETES MELLITUS, LIPOATROPHIC 2005-2006
X |
Scope note: | Inherited conditions characterized by the partial loss of ADIPOSE TISSUE, either confined to the extremities with normal or increased fat deposits on the face, neck and trunk (type 1), or confined to the loss of SUBCUTANEOUS FAT from the limbs and trunk (type 2).
X |
activeMeSHYear*: | 2007X |
dateCreated*: | 2006-07-05X |
dateEstablished*: | 2007-01-01X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | lktX |
recordOriginator*: | lktX |
Type: | |
Coordinate terms: | |
URI: | |
Labels and equivalent concepts: | Suvuittainen osittainen lipodystrofia (fi) XLipodystrophy, Familial Partial, Type 1 (en, replaced) Lipodystrophy, Familial Partial, Type 2 (en, replaced) Lipodystrophy, Familial Partial, Type 3 (en, replaced) Lipodystrophy, Familial Partial, Dunnigan Type (en, replaced) Koberling-Dunnigan Syndrome (en, replaced) Familial Partial Lipodystrophy (en, replaced) Familial Partial Lipodystrophy, Kobberling Type (en, replaced) Dunnigan Syndrome (en, replaced) |
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