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General Information
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| Term |
congenital generalized lipodystrophy type 2 |
ID (Ontology) |
DOID:0111136 (Human Disease) |
| Definition |
A congenital generalized lipodystrophy that has_material_basis_in an autosomal recessive mutation of BSCL2 on chromosome 11q12.3. |
| Also Known As |
"Berardinelli-Seip congenital lipodystrophy type 2" ; "Berardinelli-Seip syndrome" ; "Brunzell syndrome BSCL2-related" (for all, see Synonyms field below) |
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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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| 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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| Genes | Human Disease Models |
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congenital generalized lipodystrophy type 2 | 1 | 1 | for disease ribbon | congenital generalized lipodystrophy type 2 | 1 | -- | model of | congenital generalized lipodystrophy type 2 | 1 | -- |
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Relationships