Phenotypes for disease #00544 (GLUT1DS1 (GLUT1 deficiency syndrome, type 1, infantile onset, severe (GLUT1DS-1)), OMIM:606777)

9 entries on 1 page. Showing entries 1 - 9.
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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     
0000060458 GLUT1 deficiency syndrome 1 (OMIM:606777) - - Isolated (sporadic) - - - - - Daniel Trujillano 00080889
0000073824 GLUT1-deficiency - - Unknown - - - - - Andreas Laner 00037116
0000073825 GLUT1-deficiency - - Unknown - - - - - Andreas Laner 00037118
0000073826 GLUT1-deficiency syndrome, difficult epilepsy, Borderline, low CSF glucose - - Unknown - - - - - Andreas Laner 00037129
0000073827 GLUT1-deficiency: epilepsy (Absences, atonisch), ataxia, global developmental retardation, dystonia - - Unknown - - - - - Andreas Laner 00037119
0000074202 5m myoclonic seizures; severe intellectual disability (IQ ~50); “clumsy” in the mornings, with clear improvement after breakfast, but never noticed episodes that might fit with a diagnosis of paroxysmal dyskinesia - - Unknown - - - - - Erik-Jan Kamsteeg 00081421
0000078569 - - - Unknown - - - - - Johan den Dunnen 00100280
0000272305 clinically suspicion of GLUT1 deficiency syndrome - - Unknown 10y - - - - Andreas Laner 00377142
0000306883 Episodic ataxia Episodic ataxia - Unknown - - - - - Andreas Laner 00415082
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