| Tay-Sachs disease, variant AB (disorder) | | Tay-Sachs disease, variant AB | | Hexosaminidase activator deficiency
GM2 activator deficiency
AB variant
GM>2< gangliosidosis, type AB
|
| | Id | 71253000 | | Status | Primitive |
| SNOMED CT to Orphanet simple map |
| SNOMED CT to ICD-10 extended map | | Target | E75.0 | | Rule | TRUE | | Advice | ALWAYS E75.0 | | Correlation | SNOMED CT source code to target map code correlation not specified |
|
|
