Phenotypes for disease #02308 (CPT II deficiency, infantile, OMIM:600649)

3 entries on 1 page. Showing entries 1 - 3.
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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     
0000228655 - - - Familial, autosomal recessive - - - - - Helen Latsoudis 00301524
0000228656 - - - Familial, autosomal recessive - - - - - Helen Latsoudis 00301525
0000231209 Random finding of a CK elevation (> 12000U/l), no complaints, active in sports, under control CK 2684 U/l; HPO: Abnormality of the musculature - - Unknown 12y - - - - Andreas Laner 00305359
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