FCHL2
MCID: HYP333
MIFTS: 11

Hyperlipidemia, Combined, 2 (FCHL2)

Categories: Genetic diseases, Metabolic diseases, Rare diseases

Aliases & Classifications for Hyperlipidemia, Combined, 2

MalaCards integrated aliases for Hyperlipidemia, Combined, 2:

Name: Hyperlipidemia, Combined, 2 58 13 74
Hyperlipidemia, Familial Combined, 2; Fchl2 58
Hyperlipidemia, Familial Combined, 2 58
Hyplip2 58
Fchl2 58

Classifications:



External Ids:

OMIM 58 604499
MedGen 43 C1858308
UMLS 74 C1858308

Summaries for Hyperlipidemia, Combined, 2

OMIM : 58 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 EFO
18 ExPASy
20 FMA
29 GO
30 GTR
31 HGMD
32 HMDB
33 HPO
34 ICD10
35 ICD10 via Orphanet
36 ICD9CM
37 IUPHAR
38 KEGG
39 LifeMap
41 LOVD
43 MedGen
45 MeSH
46 MESH via Orphanet
47 MGI
50 NCI
51 NCIt
52 NDF-RT
55 NINDS
56 Novoseek
58 OMIM
59 OMIM via Orphanet
63 PubMed
65 QIAGEN
70 SNOMED-CT via HPO
71 SNOMED-CT via Orphanet
72 TGDB
73 Tocris
74 UMLS
75 UMLS via Orphanet
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