Phenotypes for disease #01955 (carnitine palmitoyltransferase II deficiency, late-onset, OMIM:255110)

2 entries on 1 page. Showing entries 1 - 2.
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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     
0000078455 carnitine palmitoyl transferase II deficiency myopathic form (CPT2, adult-onset form); rhabdomyolysis (HP:0003201) - - Familial, autosomal recessive - - - - - Daniela Avila-Smirnow 00095882
0000203075 - - - Familial, autosomal recessive - - - - - Jorge Docampo Cordeiro 00265254
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