GM1 gangliosidosis type 2
GM1 gangliosidosis type 2 is a clinically variable, infancy or childhood-onset form of GM1 gangliosidosis (see this term) characterized by normal early development and psychomotor regression between seven months and three years of age
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GM1 gangliosidosis type 2
Summary
GM1 gangliosidosis type 2 is a class of disease[1].
Key Facts
- GM1 gangliosidosis type 2's instance of is recorded as class of disease[2].
- GM1 gangliosidosis type 2's OMIM ID is recorded as 230600[3].
- GM1 gangliosidosis type 2's Orphanet ID is recorded as 79256[4].
- GM1 gangliosidosis type 2's genetic association is recorded as GLB1[5].
- GM1 gangliosidosis type 2's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_354[6].
- GM1 gangliosidosis type 2's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_79256[7].
- GM1 gangliosidosis type 2's UMLS CUI is recorded as C0268272[8].
- GM1 gangliosidosis type 2's UMLS CUI is recorded as C1968746[9].
- GM1 gangliosidosis type 2's ICD-10-CM is recorded as E75.1[10].
- GM1 gangliosidosis type 2's GARD rare disease ID is recorded as 10126[11].
- GM1 gangliosidosis type 2's Mondo ID is recorded as MONDO_0009261[12].
- GM1 gangliosidosis type 2's UniProt disease ID is recorded as DI-00533[13].