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1 OMIM reference -
4 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Hyperlipoproteinemia type 5
Multiple myeloma

APOA5 CCND1
CREB3L3
GPIHBP1
LPL


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
LPL
(0.63)
CCND1



Citations in the biomedical literature:


Hyperlipoproteinemia type 5
APOA5 CREB3L3 GPIHBP1 LPL
Multiple myeloma
CCND1



Hyperlipoproteinemia type 5
Multiple myeloma

Synonym(s):
- Major hyperlipidemia

Synonym(s):
- Kahler's disease
- Medullary plasmacytoma
- Myelomatosis
- Plasma cell myeloma

Classification (Orphanet):
- Inborn errors of metabolism
- Rare endocrine disease
- Rare genetic disease
Classification (Orphanet):
- Rare hematologic disease
- Rare neurologic disease
- Rare oncologic disease

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Neoplasms -

Epidemiological data:
(no data available)
Epidemiological data:
(no data available)

External references:
1 OMIM reference -
1 MeSH reference: D006954
External references:
1 OMIM reference -
1 MeSH reference: D009101

No signs/symptoms info available.