Disease #00017 (BKD (beta-ketothiolase deficiency), OMIM:607809)

Official abbreviation BKD
Name beta-ketothiolase deficiency
OMIM ID 607809
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene ACAT1
Associated tissues -
Disease features -
Remarks -

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