MCID: HYP333
MIFTS: 11

Hyperlipidemia, Combined, 2

Categories: Genetic diseases, Metabolic diseases

Aliases & Classifications for Hyperlipidemia, Combined, 2

MalaCards integrated aliases for Hyperlipidemia, Combined, 2:

Name: Hyperlipidemia, Combined, 2 57 13 73
Hyperlipidemia, Familial Combined, 2; Fchl2 57
Hyperlipidemia, Familial Combined, 2 57
Hyplip2 57
Fchl2 57

Classifications:



External Ids:

OMIM 57 604499
MedGen 42 C1858308
UMLS 73 C1858308

Summaries for Hyperlipidemia, Combined, 2

OMIM : 57 Familial combined hyperlipidemia is a common familial lipid disorder characterized by a variable pattern of elevated levels of plasma cholesterol and/or triglycerides. It is present in 10 to 20% of patients with premature coronary artery disease. (604499)

MalaCards based summary : Hyperlipidemia, Combined, 2, is also known as hyperlipidemia, familial combined, 2; fchl2. An important gene associated with Hyperlipidemia, Combined, 2 is HYPLIP2 (Hyperlipidemia, Combined, 2).

Related Diseases for Hyperlipidemia, Combined, 2

Diseases in the Hyperlipidemia, Familial Combined family:

Hyperlipidemia, Combined, 1 Hyperlipidemia, Combined, 2

Symptoms & Phenotypes for Hyperlipidemia, Combined, 2

Clinical features from OMIM:

604499

Drugs & Therapeutics for Hyperlipidemia, Combined, 2

Search Clinical Trials , NIH Clinical Center for Hyperlipidemia, Combined, 2

Genetic Tests for Hyperlipidemia, Combined, 2

Anatomical Context for Hyperlipidemia, Combined, 2

Publications for Hyperlipidemia, Combined, 2

Variations for Hyperlipidemia, Combined, 2

Expression for Hyperlipidemia, Combined, 2

Search GEO for disease gene expression data for Hyperlipidemia, Combined, 2.

Pathways for Hyperlipidemia, Combined, 2

GO Terms for Hyperlipidemia, Combined, 2

Sources for Hyperlipidemia, Combined, 2

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 ExPASy
19 FMA
28 GO
29 GTR
30 HGMD
31 HMDB
32 HPO
33 ICD10
34 ICD10 via Orphanet
35 ICD9CM
36 IUPHAR
37 KEGG
38 LifeMap
40 LOVD
42 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
54 NINDS
55 Novoseek
57 OMIM
58 OMIM via Orphanet
62 PubMed
64 QIAGEN
69 SNOMED-CT via HPO
70 SNOMED-CT via Orphanet
71 TGDB
72 Tocris
73 UMLS
74 UMLS via Orphanet
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