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GENATLAS PHENOTYPE

last update : 17-08-2009

Symbol	MTCMH10
Location	mt
Name	cardiomyopathy hypertrophic 10, neonatal
Corresponding gene	MT-ATP6 , MT-ATP8
Main clinical features	congestive heart failure with left ventricular hypertrophy, generalised weakness and delay in motor milestones, feeding difficulties
Genetic determination	mitochondrial
Function/system disorder	cardiovascular
	digestive tract/gastrointestinal
Type	disease

Remark(s)

mitochondrial m.8528TC mutation