Phenotypes for disease #01956 (CPTD1A (carnitine palmitoyltransferase deficiency, type IA), OMIM:255120)

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     
0000143399 - - - Familial, autosomal recessive - - - - - Belen Perez 00181015
0000228792 Cirrhosis - - Familial, autosomal recessive - - - - - Ponghatai Boonsimma 00301693
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