3-methylglutaconic aciduria type 7b

Summary
Definition
A 3-methylglutaconic aciduria that has_material_basis_in homozygous or compound heterozygous loss-of-function mutations in the CLPB gene on chromosome 11q13.
Super Class
3-methylglutaconic aciduria with cataracts, neurologic involvement and neutropenia
Disease Ontology
DOID:0081134
Mondo Disease Ontology
OMIM

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024