Phenotypes for disease #03048 (COXPD5 (combined oxidative phosphorylation deficiency, type 5 (COXPD-5)), OMIM:611719)

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000073487 Agenesis of corpus callosum, Hypertrophic cardiomyopathy, Pulmonary hypoplasia, Low-set ears - - Familial, autosomal recessive - - - - - Karen Stals 00095093
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