MCID: GM2001
MIFTS: 7

Gm2 Gangliosidosis, 0 Variant

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

Aliases & Classifications for Gm2 Gangliosidosis, 0 Variant

MalaCards integrated aliases for Gm2 Gangliosidosis, 0 Variant:

Name: Gm2 Gangliosidosis, 0 Variant 53

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
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
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