An instance of lipodystrophy that is caused by an inherited genomic modification in an individual.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Familial partial lipodystrophy | MONDO:0020088 | 11 | |
| Congenital generalized lipodystrophy | MONDO:0006536 | 5 | |
| Berardinelli-Seip congenital lipodystrophy | MONDO:0018883 | 4 | |
| Mandibuloacral dysplasia | MONDO:0016584 | 2 | |
| Keppen-Lubinsky syndrome | MONDO:0013572 | KCNJ6 | |
| SHORT syndrome | MONDO:0010026 | ||
| Wiedemann-Rautenstrauch syndrome | MONDO:0009910 | ||
| Lipoatrophy with diabetes, leukomelanodermic papules, liver steatosis, and hypertrophic cardiomyopathy | MONDO:0015493 | ||
| Lipodystrophy due to peptidic growth factors deficiency | MONDO:0009312 | ||
| Lipodystrophy-intellectual disability-deafness syndrome | MONDO:0011976 | ||
| Severe neurodegenerative syndrome with lipodystrophy | MONDO:0014402 | BSCL2 |
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