Disease & disorder

GM2 gangliosidosis, HEXB-related, domestic cat

MONDO:1010884

A lysosomal storage disease in cats due to a mutation in the HEXB gene. There is a buildup of GM2 gangliosides in tissues due to the lack of the enzyme hexosaminidase. Characterised by progressive neuromuscular dysfunction and impaired growth from an early age.

Outbreak surveillance

Global reported events

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Clinical trials0
Recruiting0
Drug concepts studied0
Synonyms1
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Drugs being studied

Disease identity and terminology: MONDO. Trial relationships: ClinicalTrials.gov.