Human Disease and Mouse Model Detail
|
Human Disease
|
Hypobetalipoproteinemia, Familial, 2; FHBL2
OMIM ID: 605019
|
|
Synonyms
|
Hypolipidemia, Familial, Combined
|
|
View all models
|
View ALL (2) mouse models for this human disease.
|
Genes and
mouse models
|
Mutations in human and/or mouse homologs are associated with this disease
| |
|
|
*Gene is associated with the disease in this species |
| |
|
|
 | | |
Apob*
|
APOB
|
View 2 models
|
1:1 Homology
|
 | | |
Angptl3
|
ANGPTL3*
|
|
1:1 Homology
|
|
Mouse Models
Human Disease Modeled: Hypobetalipoproteinemia, Familial, 2; FHBL2
Associated Mouse Gene:
Apob
Analysis Tools