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LMSSIO

Tay-Sachs Disease

Tay-Sachs disease is a rare, inherited neurodegenerative disorder caused by a deficiency of the enzyme hexosaminidase A. This deficiency leads to the accumulation of GM2 gangliosides, which are toxic to nerve cells.

IRI: http://lmss.sali.org/RCeiGFdK6TTSZb0MaH3Uj3P
Branch: Legal Entity
Source: https://www.ssa.gov/disability/professionals/bluebook/10.00-

Also known as

GM2 Gangliosidosis Type I, Hexosaminidase A Deficiency

Ancestry paths

Legal Entity Individual Person Characteristics Disability Physical Disability Congenital Disorders that Affect Multiple Body Systems
Legal Entity Individual Person Characteristics Disability Mental Disorders Neurocognitive Disorders

Generated from sali-legal/LMSS at 3f9ac0c9357b (2026-03-10). JSON