|
| General Information | |||
|---|---|---|---|
| Term | familial GPIHBP1 deficiency | ID (Ontology) | DOID:0111420 (Human Disease) |
| Definition | A familial chylomicronemia syndrome characterized by refactory fasting hyperchylomicronemia, and elevated plasma triglyceride levels that has_material_basis_in homozygous or compound heterozygous mutation in the GPIHBP1 gene on chromosome 8q24.3. | ||
| Also Known As | "familial glycosylphosphatidylinositol-anchored high density lipoprotein-binding protein 1 deficiency" ; "hyperlipoproteinemia type 1D" ; "hyperlipoproteinemia type ID" | ||
| Comment | |||
| Links to External Ontologies | |||
| DO.org | |||
| Annotations | |||
| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
|
|||
|
No relevant statements available
|
|||
|
||||||
autosomal genetic disease |__autosomal recessive disease________ familial hyperlipidemia | |__familial chylomicronemia syndrome__| familial GPIHBP1 deficiency |
| Spanning Tree View Settings | |||
|---|---|---|---|
| Parents/Children View Depth |
|||
Relationships
|
|||
| Is a |
autosomal recessive disease familial chylomicronemia syndrome |
||
| Part of | |||
|
Synonyms & Secondary IDs
|
|||
| Synonyms | |||
|
|||
| Secondary IDs | |||
|
|
|||
|
External Crossreferences & Linkouts
|
|||
|
MIM:615947 ORDO:535458 |
|||