Phenotypes for disease #03362 (COXPD7 (combined oxidative phosphorylation deficiency, type 7 (COXPD-7)), OMIM:613559)

1 entry on 1 page. Showing entry 1.
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     
0000060485 Combined oxidative phosphorylation deficiency 7 (OMIM:613559) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00080916
Legend   How to query  


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