MCID: GM2001
MIFTS: 7

Gm2 Gangliosidosis, 0 Variant

Categories: Rare diseases, Metabolic diseases, Bone diseases, Eye diseases, Neuronal diseases, Genetic diseases

Aliases & Classifications for Gm2 Gangliosidosis, 0 Variant

MalaCards integrated aliases for Gm2 Gangliosidosis, 0 Variant:

Name: Gm2 Gangliosidosis, 0 Variant 49

Classifications:



Summaries for Gm2 Gangliosidosis, 0 Variant

MalaCards based summary : Gm2 Gangliosidosis, 0 Variant is related to sandhoff disease.

Related Diseases for Gm2 Gangliosidosis, 0 Variant

Diseases in the Gangliosidosis Gm2 family:

Gm1-Gangliosidosis, Type I Gm1-Gangliosidosis, Type Ii
Gm1-Gangliosidosis, Type Iii Gm2-Gangliosidosis, Ab Variant
Gangliosidosis Gm1 Gm2 Gangliosidosis, 0 Variant
Gm2-Gangliosidosis, B, B1, Ab Variant

Diseases related to Gm2 Gangliosidosis, 0 Variant via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 sandhoff disease 11.7

Symptoms & Phenotypes for Gm2 Gangliosidosis, 0 Variant

Drugs & Therapeutics for Gm2 Gangliosidosis, 0 Variant

Search Clinical Trials , NIH Clinical Center for Gm2 Gangliosidosis, 0 Variant

Genetic Tests for Gm2 Gangliosidosis, 0 Variant

Anatomical Context for Gm2 Gangliosidosis, 0 Variant

Publications for Gm2 Gangliosidosis, 0 Variant

Articles related to Gm2 Gangliosidosis, 0 Variant:

# Title Authors Year
1
Molecular and structural studies of the GM2 gangliosidosis 0 variant. ( 12166653 )
2002

Variations for Gm2 Gangliosidosis, 0 Variant

Expression for Gm2 Gangliosidosis, 0 Variant

Search GEO for disease gene expression data for Gm2 Gangliosidosis, 0 Variant.

Pathways for Gm2 Gangliosidosis, 0 Variant

GO Terms for Gm2 Gangliosidosis, 0 Variant

Sources for Gm2 Gangliosidosis, 0 Variant

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
16 ExPASy
18 FMA
27 GO
28 GTR
29 HGMD
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 MedGen
41 MeSH
42 MESH via Orphanet
43 MGI
45 NCI
46 NCIt
47 NDF-RT
50 NINDS
51 Novoseek
53 OMIM
54 OMIM via Orphanet
58 PubMed
60 QIAGEN
65 SNOMED-CT via HPO
66 SNOMED-CT via Orphanet
67 TGDB
68 Tocris
69 UMLS
70 UMLS via Orphanet
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