Lipodystrophy, not elsewhere classified

Preferred Label : Lipodystrophy, not elsewhere classified;

Inclusion CIM-10 : Lipodystrophy NOS;

ICD-10 exclusion note : Whipple's disease (K90.81);

Diag associé à un acte (%) : 84.9;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

E881;

UMLS CUI

C0494360;

DO Cross reference
- congenital generalized lipodystrophy type 1 [DO Concept]
- congenital generalized lipodystrophy type 2 [DO Concept]
- congenital generalized lipodystrophy type 3 [DO Concept]
- congenital generalized lipodystrophy type 4 [DO Concept]
- lipodystrophy [DO Concept]
ICD-10 exclusion(s)
- Other intestinal malabsorption [ICD-10 Sub-category]
Manual NTBT mappings (CISMeF)
- Acquired lipodystrophy [ORDO Disease]
- Genetic lipodystrophy [ORDO Disease]
Orphanet concepts
- AKT2-related familial partial lipodystrophy [ORDO Disease]
- Acquired generalized lipodystrophy [ORDO Disease]
- Acquired lipodystrophy [ORDO Disease]
- Acquired partial lipodystrophy [ORDO Disease]
- Autosomal semi-dominant severe lipodystrophic laminopathy [ORDO Disease]
- CIDEC-related familial partial lipodystrophy [ORDO Disease]
- Centrifugal lipodystrophy [ORDO Disease]
- Congenital generalized lipodystrophy [ORDO Disease]
- Drug-induced localized lipodystrophy [ORDO Disease]
- Familial partial lipodystrophy [ORDO Disease]
- Familial partial lipodystrophy, Dunnigan type [ORDO Disease]
- Familial partial lipodystrophy, Köbberling type [ORDO Disease]
- Generalized congenital lipodystrophy with myopathy [ORDO Disease]
- Genetic lipodystrophy [ORDO Disease]
- Idiopathic localized lipodystrophy [ORDO Disease]
- Keppen-Lubinsky syndrome [ORDO Disease]
- LIPE-related familial partial lipodystrophy [ORDO Disease]
- Lipodystrophy due to peptidic growth factors deficiency [ORDO Disease]
- Localized lipodystrophy [ORDO Disease]
- PLIN1-related familial partial lipodystrophy [ORDO Disease]
- PPARG-related familial partial lipodystrophy [ORDO Disease]
- Panniculitis-induced localized lipodystrophy [ORDO Disease]
- Pressure-induced localized lipoatrophy [ORDO Disease]
- Primary lipodystrophy [ORDO Disease]
- Progeroid and marfanoid aspect-lipodystrophy syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
Validated automatic mappings to BTNT
- congenital generalized lipodystrophy type 4 [DO Concept]

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