Phenotypes for disease #03709 (COXPD10 (combined oxidative phosphorylation deficiency, type 10 (COXPD-10)), OMIM:614702)

2 entries on 1 page. Showing entries 1 - 2.
Legend   How to query  

AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000070596 2 sibs with moderate IDD, treatment resistant epileptic encephalopathy, myopathy, recurrent rhabdomyolysis; seizure improvement on ketogenic diet mitochondrial disease (respiratory chain complex I and IV deficiency) - - Familial, autosomal recessive - - - - - Johan den Dunnen 00092261
0000321074 Neurodevelopmental delay, Motor delay, Decreased activity of mitochondrial complex IV, Decreased activity of mitochondrial complex I, Hypertrophic cardiomyopathy, Intellectual disability, mild, Increased serum lactate - - Familial, autosomal recessive 08y - - - - Andreas Laner 00430266
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.