Disease #00015 (TFPD (trifunctional protein deficiency), OMIM:609015)

Official abbreviation TFPD
Name trifunctional protein deficiency
OMIM ID 609015
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 2 genes HADHA, HADHB
Associated tissues skeletal muscle
Disease features -
Remarks -

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