Disease #07123 (MTPD2 (mitochondrial trifunctional protein deficiency, type 2), OMIM:620300)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	MTPD2
Name	mitochondrial trifunctional protein deficiency, type 2
OMIM ID	620300
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	HADHB
Associated tissues	-
Disease features	-
Remarks	-
Date created	2024-11-12 15:36:08 +01:00 (CET)
Date last edited	N/A

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