| Descriptor English: | Lipodystrophy, Familial Partial | ||||||
| Descriptor Spanish: |
Lipodistrofia Parcial Familiar
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| Descriptor Portuguese: | Lipodistrofia Parcial Familiar | ||||||
| Descriptor French: | Lipodystrophie partielle familiale | ||||||
| Entry term(s): |
Dunnigan Syndrome Familial Partial Lipodystrophies Familial Partial Lipodystrophy Familial Partial Lipodystrophy, Kobberling Type Familial Partial Lipodystrophy, Type 1 Familial Partial Lipodystrophy, Type 2 Familial Partial Lipodystrophy, Type 3 Koberling Dunnigan Syndrome Koberling-Dunnigan Syndrome Lipodystrophies, Familial Partial Lipodystrophies, Reverse Partial Lipodystrophy, Familial Partial, Associated With PPARg Mutations Lipodystrophy, Familial Partial, Dunnigan Type Lipodystrophy, Familial Partial, Kobberling Type Lipodystrophy, Familial Partial, Type 1 Lipodystrophy, Familial Partial, Type 2 Lipodystrophy, Familial Partial, Type 3 Lipodystrophy, Familial, of Limbs and Lower Trunk Lipodystrophy, Reverse Partial Partial Lipodystrophies, Familial Partial Lipodystrophies, Reverse Partial Lipodystrophy, Familial Partial Lipodystrophy, Reverse Reverse Partial Lipodystrophies Reverse Partial Lipodystrophy Syndrome, Dunnigan |
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| Tree number(s): |
C16.320.488.813 C17.800.849.391.700 C18.452.584.563.798 C18.452.584.625.700 C18.452.880.391.700 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D052496 | ||||||
| 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). Type 3 is associated with mutation in the gene encoding PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR GAMMA. |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Previous Indexing: |
Lipodystrophy (1975-2006) |
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| Public MeSH Note: | 2007; see DIABETES MELLITUS, LIPOATROPHIC 2005-2006 |
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| History Note: | 2007; use DIABETES MELLITUS, LIPOATROPHIC 2005-2006 |
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| Related: |
PPAR gamma
MeSH | ||||||
| DeCS ID: | 52150 | ||||||
| Unique ID: | D052496 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 2007/01/01 | ||||||
| Date of Entry: | 2006/07/05 | ||||||
| Revision Date: | 2012/07/03 |
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Lipodystrophy, Familial Partial
- Preferred
Familial Partial Lipodystrophy, Type 2
- Narrower
Familial Partial Lipodystrophy, Type 3
- Narrower
Familial Partial Lipodystrophy, Type 1
- Narrower
| Concept UI |
M0462327 |
| 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). Type 3 is associated with mutation in the gene encoding PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR GAMMA. |
| Preferred term | Lipodystrophy, Familial Partial |
| Entry term(s) |
Familial Partial Lipodystrophies Familial Partial Lipodystrophy Koberling Dunnigan Syndrome Koberling-Dunnigan Syndrome Lipodystrophies, Familial Partial Partial Lipodystrophies, Familial Partial Lipodystrophy, Familial |
| Concept UI |
M0487302 |
| Scope note | This type can be caused by mutation in the gene encoding LAMIN TYPE A. |
| Preferred term | Familial Partial Lipodystrophy, Type 2 |
| Entry term(s) |
Dunnigan Syndrome Lipodystrophies, Reverse Partial Lipodystrophy, Familial Partial, Dunnigan Type Lipodystrophy, Familial Partial, Type 2 Lipodystrophy, Familial, of Limbs and Lower Trunk Lipodystrophy, Reverse Partial Partial Lipodystrophies, Reverse Partial Lipodystrophy, Reverse Reverse Partial Lipodystrophies Reverse Partial Lipodystrophy Syndrome, Dunnigan |
| Concept UI |
M0487304 |
| Scope note | This type can be caused by mutation in the gene encoding PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR GAMMA. |
| Preferred term | Familial Partial Lipodystrophy, Type 3 |
| Entry term(s) |
Lipodystrophy, Familial Partial, Associated With PPARg Mutations Lipodystrophy, Familial Partial, Type 3 |
| Concept UI |
M0487303 |
| Preferred term | Familial Partial Lipodystrophy, Type 1 |
| Entry term(s) |
Familial Partial Lipodystrophy, Kobberling Type Lipodystrophy, Familial Partial, Kobberling Type Lipodystrophy, Familial Partial, Type 1 |
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