MCID: MYH013
MIFTS: 5

Myh7-Related Congenital Fiber-Type Disproportion malady

Categories: Genetic diseases, Rare diseases, Neuronal diseases, Muscle diseases

Aliases & Classifications for Myh7-Related Congenital Fiber-Type Disproportion

Aliases & Descriptions for Myh7-Related Congenital Fiber-Type Disproportion:

Name: Myh7-Related Congenital Fiber-Type Disproportion 24

Classifications:



Summaries for Myh7-Related Congenital Fiber-Type Disproportion

MalaCards based summary : Myh7-Related Congenital Fiber-Type Disproportion An important gene associated with Myh7-Related Congenital Fiber-Type Disproportion is MYH7 (Myosin Heavy Chain 7).

Related Diseases for Myh7-Related Congenital Fiber-Type Disproportion

Symptoms & Phenotypes for Myh7-Related Congenital Fiber-Type Disproportion

Drugs & Therapeutics for Myh7-Related Congenital Fiber-Type Disproportion

Search Clinical Trials , NIH Clinical Center for Myh7-Related Congenital Fiber-Type Disproportion

Genetic Tests for Myh7-Related Congenital Fiber-Type Disproportion

Genetic tests related to Myh7-Related Congenital Fiber-Type Disproportion:

id Genetic test Affiliating Genes
1 Myh7-Related Congenital Fiber-Type Disproportion 24 MYH7

Anatomical Context for Myh7-Related Congenital Fiber-Type Disproportion

Publications for Myh7-Related Congenital Fiber-Type Disproportion

Variations for Myh7-Related Congenital Fiber-Type Disproportion

Expression for Myh7-Related Congenital Fiber-Type Disproportion

Search GEO for disease gene expression data for Myh7-Related Congenital Fiber-Type Disproportion.

Pathways for Myh7-Related Congenital Fiber-Type Disproportion

GO Terms for Myh7-Related Congenital Fiber-Type Disproportion

Sources for Myh7-Related Congenital Fiber-Type Disproportion

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
16 ExPASy
18 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 MedGen
42 MeSH
43 MESH via Orphanet
44 MGI
46 NCI
47 NCIt
48 NDF-RT
51 NINDS
52 Novoseek
54 OMIM
55 OMIM via Orphanet
59 PubMed
60 QIAGEN
65 SNOMED-CT via Orphanet
67 TGDB
68 Tocris
69 UMLS
70 UMLS via Orphanet
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