Phenotypes for disease #00172 (SBCADD (2-methylbutyryl-CoA dehydrogenase deficiency (SBCADD)), OMIM:610006)

24 entries on 1 page. Showing entries 1 - 24.
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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     
0000000897 - Unknown - - - - newborn screening - - Division of Human Genetics, Innsbruck 00001743
0000000898 - Unknown - - - - family analysis; no clinical symptoms - - Division of Human Genetics, Innsbruck 00001744
0000000899 - Unknown - - - - clinical presentation - - Division of Human Genetics, Innsbruck 00001745
0000000900 - Unknown - - - - newborn screening - - Division of Human Genetics, Innsbruck 00001746
0000000901 - Unknown - - - - family analysis - - Division of Human Genetics, Innsbruck 00001747
0000000902 - Unknown - - - - newborn screening - - Division of Human Genetics, Innsbruck 00001748
0000000903 - Unknown - - - - newborn screening - - Division of Human Genetics, Innsbruck 00001749
0000000904 - Unknown - - - - family analysis - - Division of Human Genetics, Innsbruck 00001750
0000000905 - Unknown - - - - newborn screening - - Division of Human Genetics, Innsbruck 00001751
0000000906 - Unknown - - - - unknown - - Division of Human Genetics, Innsbruck 00001752
0000000907 - Unknown - - - - unknown - - Division of Human Genetics, Innsbruck 00001753
0000000908 - Unknown - - - - unknown - - Division of Human Genetics, Innsbruck 00001754
0000000909 - Unknown - - - - newborn screening; no clinical symptoms - - Division of Human Genetics, Innsbruck 00001755
0000000910 - Unknown - - - - newborn screening; no clinical symptoms - - Division of Human Genetics, Innsbruck 00001756
0000000911 - Unknown - - - - newborn screening; no clinical symptoms - - Division of Human Genetics, Innsbruck 00001757
0000000912 - Unknown - - - - clinical presentation; developmental delay, simplified brain sulci pattern, microcephaly - - Division of Human Genetics, Innsbruck 00001758
0000000913 - Unknown - - - - newborn screening - - Division of Human Genetics, Innsbruck 00001759
0000000914 - Familial - - 00y05m - clinical presentation; seizures (which stopped), speech development was significantly delayed, mental retardation - 04y Division of Human Genetics, Innsbruck 00001760
0000000915 - Familial - - 00y06m - clinical presentation; seizures (which stopped from 10 months onwards), develompmental delay, hypotonia - 00y06m Division of Human Genetics, Innsbruck 00001761
0000000916 - Familial - - 00y00m03d - clinical presentation; developmental delay, epilepsy - - Division of Human Genetics, Innsbruck 00001762
0000000917 - Unknown - - - - newborn screening - - Division of Human Genetics, Innsbruck 00001763
0000000918 - Unknown - - - - newborn screening - - Division of Human Genetics, Innsbruck 00001764
0000000919 - Familial - - - - family analysis; no clinical symptoms - - Division of Human Genetics, Innsbruck 00001765
0000143307 - Familial, autosomal recessive - - - - - - - Belen Perez 00181054
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