MCID: CNM001
MIFTS: 14

Canomad Syndrome

Categories: Immune diseases, Neuronal diseases, Rare diseases

Aliases & Classifications for Canomad Syndrome

MalaCards integrated aliases for Canomad Syndrome:

Name: Canomad Syndrome 54 60 74
Chronic Ataxic Neuropathy-Ophthalmoplegia-Igm Paraprotein-Cold Agglutinins-Disialosyl Antibodies Syndrome 60
Chronic Ataxic Neuropathy Ophthalmoplegia M-Protein Agglutination Disialosyl Antibodies Syndrome 54
Chronic Sensory Ataxic Neuropathy with Anti-Disialosyl Igm Antibodies 60
Chronic Sensory Ataxic Neuropathy with Anti-Disialosyl Antibodies 54
Canda Syndrome 60

Characteristics:

Orphanet epidemiological data:

60
canomad syndrome
Age of onset: Adult;

Classifications:

Orphanet: 60  
Rare neurological diseases


External Ids:

MESH via Orphanet 46 C537980
ICD10 via Orphanet 35 G61.8
UMLS via Orphanet 75 C2931684
Orphanet 60 ORPHA71279
UMLS 74 C2931684

Summaries for Canomad Syndrome

NIH Rare Diseases : 54 CANOMAD syndrome is a rare chronic immune-mediated demyelinating polyneuropathy. CANOMAD stands for Chronic Ataxic Neuropathy Ophthalmoplegia IgM paraprotein Cold Agglutinins Disialosyl antibodies. Signs and symptoms of CANOMAD may include loss of muscle, tendon, and joint sensation, abnormal gait (walk), ataxia, tingling sensation on the skin around the mouth or extremities, paralysis of eye muscles, difficulty swallowing and speaking, and rarely respiratory muscle weakness. This condition is caused by the presence of anti-diasialosyl antibodies in the body.  Oral or intravenous corticosteroids, �?-interferons, plasma exchange, intravenous immunoglobulin (IVIG), and cytotoxic drugs have all been used in treating CANOMAD with varying success.

MalaCards based summary : Canomad Syndrome, is also known as chronic ataxic neuropathy-ophthalmoplegia-igm paraprotein-cold agglutinins-disialosyl antibodies syndrome, and has symptoms including ataxia and ophthalmoplegia. Affiliated tissues include skin and eye.

Related Diseases for Canomad Syndrome

Symptoms & Phenotypes for Canomad Syndrome

UMLS symptoms related to Canomad Syndrome:


ataxia, ophthalmoplegia

Drugs & Therapeutics for Canomad Syndrome

Search Clinical Trials , NIH Clinical Center for Canomad Syndrome

Genetic Tests for Canomad Syndrome

Anatomical Context for Canomad Syndrome

MalaCards organs/tissues related to Canomad Syndrome:

42
Skin, Eye

Publications for Canomad Syndrome

Articles related to Canomad Syndrome:

# Title Authors Year
1
Corrigendum to "A case of false positive cardiac troponin I in CANOMAD syndrome" [Int. J. Cardiol. 222 (2016) 359-360]. ( 29499853 )
2018
2
A case of false positive cardiac troponin I in CANOMAD syndrome. ( 27500764 )
2016

Variations for Canomad Syndrome

Expression for Canomad Syndrome

Search GEO for disease gene expression data for Canomad Syndrome.

Pathways for Canomad Syndrome

GO Terms for Canomad Syndrome

Sources for Canomad Syndrome

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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