Disease #00119 (MC2DN4 (MITOCHONDRIAL COMPLEX II DEFICIENCY, NUCLEAR TYPE 4), OMIM:619224)

Official abbreviation	MC2DN4
Name	MITOCHONDRIAL COMPLEX II DEFICIENCY, NUCLEAR TYPE 4
OMIM ID	619224
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SDHB
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-06-16 10:07:02 +00:00 (UTC)
Date last edited	N/A

MVZ für Humangenetik Regensburg