MCID: CNG441
MIFTS: 14

Congenital Muscular Dystrophy Due to Dystroglycanopathy

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

Aliases & Classifications for Congenital Muscular Dystrophy Due to Dystroglycanopathy

MalaCards integrated aliases for Congenital Muscular Dystrophy Due to Dystroglycanopathy:

Name: Congenital Muscular Dystrophy Due to Dystroglycanopathy 53
Cmd Due to Dystroglycanopathy 53
Dystroglycanopathy 53

Classifications:



Summaries for Congenital Muscular Dystrophy Due to Dystroglycanopathy

MalaCards based summary : Congenital Muscular Dystrophy Due to Dystroglycanopathy, also known as cmd due to dystroglycanopathy, is related to muscular dystrophy-dystroglycanopathy , type a, 4 and muscular dystrophy-dystroglycanopathy , type c, 3. The drugs Immunologic Factors and Immunoglobulins, Intravenous have been mentioned in the context of this disorder. Affiliated tissues include bone, brain and eye.

Related Diseases for Congenital Muscular Dystrophy Due to Dystroglycanopathy

Diseases in the Muscular Dystrophy family:

Muscular Dystrophy, Congenital, 1b Muscular Dystrophy, Congenital, Lmna-Related
Lama2-Related Muscular Dystrophy Congenital Muscular Dystrophy Due to Dystroglycanopathy
Congenital Muscular Dystrophy Type 1a

Diseases related to Congenital Muscular Dystrophy Due to Dystroglycanopathy via text searches within MalaCards or GeneCards Suite gene sharing:

(show top 50) (show all 55)
# Related Disease Score Top Affiliating Genes
1 muscular dystrophy-dystroglycanopathy , type a, 4 12.4
2 muscular dystrophy-dystroglycanopathy , type c, 3 12.4
3 muscular dystrophy-dystroglycanopathy , type c, 2 12.4
4 muscular dystrophy-dystroglycanopathy , type c, 9 12.4
5 muscular dystrophy-dystroglycanopathy , type c, 14 12.4
6 muscular dystrophy-dystroglycanopathy , type c, 1 12.4
7 muscular dystrophy-dystroglycanopathy , type c, 5 12.4
8 muscular dystrophy-dystroglycanopathy , type b, 4 12.4
9 muscular dystrophy-dystroglycanopathy , type b, 1 12.4
10 muscular dystrophy-dystroglycanopathy , type b, 5 12.4
11 muscular dystrophy-dystroglycanopathy , type b, 6 12.4
12 muscular dystrophy-dystroglycanopathy , type a, 8 12.4
13 muscular dystrophy-dystroglycanopathy , type a, 11 12.4
14 muscular dystrophy-dystroglycanopathy , type a, 2 12.4
15 muscular dystrophy-dystroglycanopathy , type a, 5 12.4
16 muscular dystrophy-dystroglycanopathy , type a, 6 12.4
17 muscular dystrophy-dystroglycanopathy , type a, 7 12.4
18 muscular dystrophy-dystroglycanopathy , type a, 10 12.4
19 muscular dystrophy-dystroglycanopathy , type a, 12 12.4
20 muscular dystrophy-dystroglycanopathy , type a, 3 12.3
21 muscular dystrophy-dystroglycanopathy , type a, 13 12.3
22 muscular dystrophy-dystroglycanopathy , type b, 3 12.3
23 muscular dystrophy-dystroglycanopathy , type b, 2 12.3
24 muscular dystrophy-dystroglycanopathy , type a, 9 12.3
25 muscular dystrophy-dystroglycanopathy , type c, 4 12.3
26 muscular dystrophy-dystroglycanopathy , type a, 1 12.3
27 muscular dystrophy-dystroglycanopathy , type b, 14 12.3
28 muscular dystrophy-dystroglycanopathy , type c, 7 12.3
29 muscular dystrophy-dystroglycanopathy , type c, 12 12.3
30 muscular dystrophy-dystroglycanopathy , type a, 14 12.3
31 muscular dystrophy-dystroglycanopathy , type c, 8 12.3
32 muscular dystrophy-dystroglycanopathy , type c, 15 11.9
33 congenital muscular alpha-dystroglycanopathy with brain and eye anomalies 11.9
34 congenital muscular dystrophy-dystroglycanopathy with or without intellectual disability 11.9
35 walker-warburg syndrome 11.5
36 muscle eye brain disease 11.4
37 muscular dystrophy-dystroglycanopathy 11.4
38 fukuyama type muscular dystrophy 11.3
39 congenital disorder of glycosylation, type ie 10.9
40 congenital muscular dystrophy without intellectual disability 10.9
41 muscular dystrophy 10.6
42 muscular dystrophy, congenital, lmna-related 10.4
43 limb-girdle muscular dystrophy 10.2
44 epilepsy 10.1
45 marinesco-sjogren syndrome 10.0
46 sjogren syndrome 10.0
47 congenital disorder of glycosylation, type in 10.0
48 alacrima, achalasia, and mental retardation syndrome 10.0
49 polyglucosan body myopathy 1 with or without immunodeficiency 10.0
50 ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus 10.0

Graphical network of the top 20 diseases related to Congenital Muscular Dystrophy Due to Dystroglycanopathy:



Diseases related to Congenital Muscular Dystrophy Due to Dystroglycanopathy

Symptoms & Phenotypes for Congenital Muscular Dystrophy Due to Dystroglycanopathy

Drugs & Therapeutics for Congenital Muscular Dystrophy Due to Dystroglycanopathy

Drugs for Congenital Muscular Dystrophy Due to Dystroglycanopathy (from DrugBank, HMDB, Dgidb, PharmGKB, IUPHAR, NovoSeek, BitterDB):

(show all 6)
# Name Status Phase Clinical Trials Cas Number PubChem Id
1 Immunologic Factors Phase 1
2 Immunoglobulins, Intravenous Phase 1
3 gamma-Globulins Phase 1
4 Immunoglobulins Phase 1
5 Antibodies Phase 1
6 Rho(D) Immune Globulin Phase 1

Interventional clinical trials:


# Name Status NCT ID Phase Drugs
1 Intravenous Immune Globulin to Treat Hereditary Inclusion Body Myopathy Completed NCT00195637 Phase 1 Immune Globulin
2 Clinical Trial Readiness for the Dystroglycanopathies Recruiting NCT00313677
3 Congenital Muscle Disease Study of Patient and Family Reported Medical Information Recruiting NCT01403402

Search NIH Clinical Center for Congenital Muscular Dystrophy Due to Dystroglycanopathy

Genetic Tests for Congenital Muscular Dystrophy Due to Dystroglycanopathy

Anatomical Context for Congenital Muscular Dystrophy Due to Dystroglycanopathy

MalaCards organs/tissues related to Congenital Muscular Dystrophy Due to Dystroglycanopathy:

41
Bone, Brain, Eye

Publications for Congenital Muscular Dystrophy Due to Dystroglycanopathy

Variations for Congenital Muscular Dystrophy Due to Dystroglycanopathy

Expression for Congenital Muscular Dystrophy Due to Dystroglycanopathy

Search GEO for disease gene expression data for Congenital Muscular Dystrophy Due to Dystroglycanopathy.

Pathways for Congenital Muscular Dystrophy Due to Dystroglycanopathy

GO Terms for Congenital Muscular Dystrophy Due to Dystroglycanopathy

Sources for Congenital Muscular Dystrophy Due to Dystroglycanopathy

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
Content
Loading form....