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Human Disease and Mouse Model Detail
Human Disease Hypoalphalipoproteinemia, Primary
OMIM ID: 604091
Synonyms Familial Hdl Deficiency; FHD; Hdl Cholesterol, Low Serum; HDLC; High Density Lipoprotein Deficiency; HDLD; Hypoalphalipoproteinemia, Familial; FHA
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
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     Abca1 ABCA1*   1:1 Homology
Apoa1 APOA1*   1:1 Homology

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
11/18/2014
MGI 5.20
The Jackson Laboratory