MCID: MLT168
MIFTS: 12

Multicore Disease

Categories: Rare diseases

Aliases & Classifications for Multicore Disease

MalaCards integrated aliases for Multicore Disease:

Name: Multicore Disease 20
Multiocre Myopathy 20

Classifications:



Summaries for Multicore Disease

MalaCards based summary : Multicore Disease, also known as multiocre myopathy, is related to multiminicore disease and myopathy. An important gene associated with Multicore Disease is RYR1 (Ryanodine Receptor 1). Affiliated tissues include pituitary, skeletal muscle and endothelial.

Related Diseases for Multicore Disease

Graphical network of the top 20 diseases related to Multicore Disease:



Diseases related to Multicore Disease

Symptoms & Phenotypes for Multicore Disease

Drugs & Therapeutics for Multicore Disease

Search Clinical Trials , NIH Clinical Center for Multicore Disease

Genetic Tests for Multicore Disease

Anatomical Context for Multicore Disease

MalaCards organs/tissues related to Multicore Disease:

40
Pituitary, Skeletal Muscle, Endothelial

Publications for Multicore Disease

Articles related to Multicore Disease:

(show all 39)
# Title Authors PMID Year
1
Significance of Asymptomatic Hyper Creatine-Kinase Emia. 61
31743252 2019
2
Congenital myopathies: clinical and immunohistochemical study. 61
22234203 2011
3
Dominant and recessive RYR1 mutations in adults with core lesions and mild muscle symptoms. 61
21674524 2011
4
Surgery for foot deformity in patients with congenital myopathy (multicore disease, congenital fiber-type disproportion, and centronuclear myopathy). 61
19483656 2009
5
Mivacurium in multicore disease. 61
16802504 2006
6
Myalgia as the revealing symptom of multicore disease and fibre type disproportion myopathy. 61
12933945 2003
7
The significance of type 1 fiber atrophy (hypotrophy) in childhood neuromuscular disorders. 61
11504599 2001
8
[Central core disease, multicore disease, minicore disease]. 61
11555967 2001
9
Rapidly progredient scoliosis associated with multicore disease. 61
9709867 1998
10
Discordant light microscopic, electron microscopic, and in vitro contracture study findings in a family with central core disease. 61
9323448 1997
11
The respiratory muscles in multicore myopathy. 61
8317804 1993
12
A family with multicore disease. 61
8515769 1993
13
[Multicore disease with pulmonary and heart failure caused by acute pneumonia--a case report]. 61
1731833 1992
14
Asymptomatic hyper-CK-emia: an electrophysiologic and histopathologic study. 61
2725551 1989
15
The rigid spine syndrome in two sisters. 61
3351513 1988
16
Minicore myopathy with dominant inheritance. 61
3806134 1987
17
Severe multicore disease associated with reaction to anesthesia. 61
4062619 1985
18
"Central core" and "multicore" disease. Clinical, histochemical and ultrastructural study of two cases with unusual hereditary transmission. 61
4091061 1985
19
Multicore disease and Marfan's syndrome: a case report. 61
3996454 1985
20
Multicore disease in sibs with severe mental retardation, short stature, facial anomalies, hypoplasia of the pituitary fossa, and hypogonadotrophic hypogonadism. 61
3970066 1985
21
Familial myopathy associated with Marfanoid features and multicores. 61
6596064 1984
22
Endothelial alterations of skeletal muscle capillaries in childhood myopathies. 61
6636137 1983
23
Myopathy with pathological features of both centronuclear myopathy and multicore disease. 61
7161626 1982
24
Autosomal dominant multicore disease. 61
7077346 1982
25
Coexistence of minicores, cores, and rods in the same muscle biopsy. A new example of mixed congenital myopathy. 61
7158301 1982
26
Familial multicore disease with focal loss of cross-striations and ophthalmoplegia. 61
7299413 1981
27
A fatal congenital myopathy with severe type I fibre atrophy, central nuclei and multicores. 61
7229670 1981
28
A study of a myopathy presenting as idiopathic scoliosis. Multicore disease or mitochondrial myopathy? 61
7373343 1980
29
Congenital non-progressive myopathy, associated with scoliosis--clinical, histological, histochemical and electron microscopic studies of seven cases. 61
7391631 1980
30
Multicore disease. 61
7368023 1980
31
Mixed nemaline-mitochondrial "myopathy". 61
6255722 1980
32
Familial multicore disease. 61
553390 1979
33
Multicore disease. Report of a case with lack of fibre type differentiation. 61
213746 1978
34
[Central core disease and multicore disease]. 61
691505 1978
35
Central core disease: histochemical and ultrastructural study of muscle biopsies of father and daughter. 61
77319 1978
36
Multicore disease in twins. 61
985853 1976
37
Multicore disease: report of a case with onset in middle age. 61
4153807 1974
38
[Multicore disease]. 61
4737762 1973
39
Multicore disease. A recently recognized congenital myopathy associated with multifocal degeneration of muscle fibers. 61
5115748 1971

Variations for Multicore Disease

Expression for Multicore Disease

Search GEO for disease gene expression data for Multicore Disease.

Pathways for Multicore Disease

GO Terms for Multicore Disease

Sources for Multicore Disease

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
20 GARD
28 GO
29 GTR
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 LOVD
41 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
53 NINDS
54 Novoseek
56 OMIM via Orphanet
57 OMIM® (Updated 20-May-2021)
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 Tocris
70 UMLS
71 UMLS via Orphanet
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