Phenotypes for disease #01881 (SCOTD (succinyl-CoA acetoacetate transferase deficiency (SCOTD)), OMIM:245050)

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     
0000060528 Succinyl CoA:3-oxoacid CoA transferase deficiency (OMIM:245050) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00080959
0000171699 - - SCOTD Familial, autosomal recessive - - 7m - - Toshiyuki Fukao 00226587
0000340279 Attention deficit hyperactivity disorder, mild intellectual disability, seizures Succinyl CoA:3-oxoacid CoA transferase deficiency Succinyl CoA:3-oxoacid CoA transferase deficiency Familial, autosomal recessive - 02y - - - Miriam Erandi Reyna-Fabián 00451603
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