GM1 gangliosidosis type 1
GM1 gangliosidosis type 1 is the severe infantile form of GM1 gangliosidosis (see this term) with variable neurological and systemic manifestations
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GM1 gangliosidosis type 1
Summary
GM1 gangliosidosis type 1 is a class of disease[1].
Key Facts
- GM1 gangliosidosis type 1's instance of is recorded as class of disease[2].
- GM1 gangliosidosis type 1's subclass of is recorded as gangliosidosis GM1[3].
- GM1 gangliosidosis type 1's OMIM ID is recorded as 230500[4].
- GM1 gangliosidosis type 1's Disease Ontology ID is recorded as DOID:0080502[5].
- GM1 gangliosidosis type 1's symptoms and signs is recorded as hepatosplenomegaly[6].
- GM1 gangliosidosis type 1's Orphanet ID is recorded as 79255[7].
- GM1 gangliosidosis type 1's genetic association is recorded as GLB1[8].
- GM1 gangliosidosis type 1's Google Knowledge Graph ID is recorded as /g/11b6f50ght[9].
- GM1 gangliosidosis type 1's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_79255[10].
- GM1 gangliosidosis type 1's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080502[11].
- GM1 gangliosidosis type 1's exact match is recorded as http://identifiers.org/doid/DOID:0080502[12].
- GM1 gangliosidosis type 1's UMLS CUI is recorded as C1968748[13].
- GM1 gangliosidosis type 1's UMLS CUI is recorded as C0268271[14].
- GM1 gangliosidosis type 1's ICD-10-CM is recorded as E75.1[15].
- GM1 gangliosidosis type 1's GARD rare disease ID is recorded as 6479[16].
- GM1 gangliosidosis type 1's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].
- GM1 gangliosidosis type 1's Mondo ID is recorded as MONDO_0009260[18].
- GM1 gangliosidosis type 1's UniProt disease ID is recorded as DI-00532[19].