Phenotypes for disease #00171 (IBDD (isobutyryl-CoA dehydrogenase deficiency (IBDD)), OMIM:611283)

25 entries on 1 page. Showing entries 1 - 25.
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AscendingPhenotype ID     

Diagnosis/Initial     

Inheritance     

Age/Examination     

Diagnosis/Definite     

Age/Onset     

Phenotype/Onset     

Phenotype details     

Protein     

Age/Diagnosis     

Owner     

Individual ID     
0000000873 - Familial - - - - no clinical phenotype at age of diagnosis - 00y03m Division of Human Genetics, Innsbruck 00001719
0000000874 - Unknown - - - - ascertainment unknown - - Division of Human Genetics, Innsbruck 00001720
0000000875 - Familial - - - - ascertainment clinical presentation - - Division of Human Genetics, Innsbruck 00001721
0000000876 - Familial - - - - ascertainment clinical presentation - - Division of Human Genetics, Innsbruck 00001722
0000000877 - Unknown - - - - ascertainment clinical presentation - - Division of Human Genetics, Innsbruck 00001723
0000000878 - Unknown - - - - ascertainment newborn screening - - Division of Human Genetics, Innsbruck 00001724
0000000879 - Unknown - - - - ascertainment newborn screening - - Division of Human Genetics, Innsbruck 00001725
0000000880 - Unknown - - - - ascertainment newborn screening - - Division of Human Genetics, Innsbruck 00001726
0000000881 - Unknown - - - - ascertainment newborn screening - - Division of Human Genetics, Innsbruck 00001727
0000000882 - Unknown - - - - ascertainment clinical presentation - 2y Division of Human Genetics, Innsbruck 00001728
0000000883 - Unknown - - - - ascertainment newborn screening - 00y00m18d Division of Human Genetics, Innsbruck 00001729
0000000884 - Unknown - - - - ascertainment unknown - - Division of Human Genetics, Innsbruck 00001730
0000000885 - Unknown - - - - ascertainment unknown - - Division of Human Genetics, Innsbruck 00001731
0000000886 - Unknown - - - - ascertainment newborn screening - 00y00m09d Division of Human Genetics, Innsbruck 00001732
0000000887 - Unknown - - - - - - 00y03m Division of Human Genetics, Innsbruck 00001733
0000000888 - Unknown - - - - ascertainment newborn screening - 00y00m05d Division of Human Genetics, Innsbruck 00001734
0000000889 - Unknown - - - - ascertainment newborn screening - 00y00m14d Division of Human Genetics, Innsbruck 00001735
0000000890 - Unknown - - - - ascertainment newborn screening - 00y00m16d Division of Human Genetics, Innsbruck 00001736
0000000891 - Unknown - - - - ascertainment newborn screening - 00y00m07d Division of Human Genetics, Innsbruck 00001737
0000000892 - Unknown - - - - ascertainment newborn screening - 00y00m42d Division of Human Genetics, Innsbruck 00001738
0000000893 - Unknown - - - - ascertainment newborn screening - 00y02m Division of Human Genetics, Innsbruck 00001739
0000000894 - Unknown - - - - ascertainment newborn screening - 00y00m21d Division of Human Genetics, Innsbruck 00001740
0000000895 - Familial - - - - ascertainment newborn screening; additionally affected with glutaric aciduria type 1 - 00y00m01d Division of Human Genetics, Innsbruck 00001741
0000000896 - Unknown - - - - ascertainment newborn screening - 00y00m09d Division of Human Genetics, Innsbruck 00001742
0000143265 - Familial, autosomal recessive - - - - - - - Belen Perez 00181001
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