gangliosidosis, generalized GM1, Late-Infantile type

Preferred Label : gangliosidosis, generalized GM1, Late-Infantile type;

MeSH note : mutation in beta-galactosidase-1;

Origin ID

C566893;

UMLS CUI

C1968746;

Automatic exact mappings (from CISMeF team)
- Gm1-gangliosidosis, type II [OMIM Phenotype]
MeSH term(s) associated for indexing
- gangliosidosis, GM1 [MeSH Descriptor]
Record concept(s)
- gangliosidosis, generalized GM1, Late-Infantile type [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]