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General Information
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| Term |
congenital generalized lipodystrophy |
ID (Ontology) |
DOID:0050585 (Human Disease) |
| Definition |
A lipodystrophy that is characterized by extreme scarcity of subcutaneous fat, muscular hypertrophy, fatty liver, hypertriglyceremia and metabolic complications including insulin resistance. |
| Comment |
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Links to External Ontologies
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DO.org
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Annotations
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Records annotated with this term OR any of its CHILD TERMS
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Records annotated with this exact term (annotations to child terms are NOT included)
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| Data Class | Field | Records |
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| Alleles (FBal) | HUMAN_DISEASE_INTERACTIONS | 11 | | Human Disease Models (FBhh) | DOID | 1 |
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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| Full annotation statements | Relevant FlyBase reports |
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| Alleles | Genes | Human Disease Models |
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congenital generalized lipodystrophy | 11 | 7 | 1 | ameliorates | congenital generalized lipodystrophy | 6 | -- | -- | exacerbates | congenital generalized lipodystrophy | 5 | -- | -- | model of | congenital generalized lipodystrophy | 2 | -- | -- |
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Relationships