gangliosidosis GM1
lysosomal storage disease
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gangliosidosis GM1
Summary
gangliosidosis GM1 is a rare disease[1]. It is known by 9 alternative names across languages and contexts.[2]
Key Facts
- gangliosidosis GM1's instance of is recorded as rare disease[3].
- gangliosidosis GM1's instance of is recorded as class of disease[4].
- gangliosidosis GM1 is a type of gangliosidosis[5].
- gangliosidosis GM1 is a type of neurometabolic disease[6].
- gangliosidosis GM1 is a type of lysosomal storage disease with skeletal involvement[7].
- gangliosidosis GM1 is a type of hereditary retinal dystrophy[8].
- gangliosidosis GM1 is a type of metabolic disease with macular cherry-red spot[9].
- gangliosidosis GM1 is a type of nervous system anomaly with eye involvement[10].
- gangliosidosis GM1 is a type of unclassified primitive or secondary maculopathy[11].
- gangliosidosis GM1's ICD-9-CM is recorded as 277.6[12].
- gangliosidosis GM1's NCI Thesaurus ID is recorded as C84739[13].
- gangliosidosis GM1's health specialty is recorded as endocrinology[14].
- gangliosidosis GM1's genetic association is recorded as GLB1[15].
- gangliosidosis GM1's exact match is recorded as http://purl.obolibrary.org/obo/DOID_3322[16].
- gangliosidosis GM1's exact match is recorded as http://identifiers.org/doid/DOID:3322[17].
- gangliosidosis GM1's exact match is recorded as http://purl.obolibrary.org/obo/HP_0008166[18].
- gangliosidosis GM1's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_354[19].
- gangliosidosis GM1's on focus list of Wikimedia project is recorded as WikiProject Medicine[20].
Why It Matters
gangliosidosis GM1 is known by 9 alternative names across languages and contexts.[2]