GM1 gangliosidosis type 3
GM1 gangliosidosis type 3 is a mild, chronic, adult form of GM1 gangliosidosis (see this term) characterized by onset generally during childhood or adolescence and by cerebellar dysfunction
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GM1 gangliosidosis type 3
Summary
GM1 gangliosidosis type 3 is a class of disease[1].
Key Facts
- GM1 gangliosidosis type 3's instance of is recorded as class of disease[2].
- GM1 gangliosidosis type 3's OMIM ID is recorded as 230650[3].
- GM1 gangliosidosis type 3's Orphanet ID is recorded as 79257[4].
- GM1 gangliosidosis type 3's genetic association is recorded as GLB1[5].
- GM1 gangliosidosis type 3's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_354[6].
- GM1 gangliosidosis type 3's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_79257[7].
- GM1 gangliosidosis type 3's UMLS CUI is recorded as C0268273[8].
- GM1 gangliosidosis type 3's ICD-10-CM is recorded as E75.1[9].
- GM1 gangliosidosis type 3's GARD rare disease ID is recorded as 2431[10].
- GM1 gangliosidosis type 3's Mondo ID is recorded as MONDO_0009262[11].
- GM1 gangliosidosis type 3's UniProt disease ID is recorded as DI-00534[12].