Disease #00037 (TSC (Tuberous sclerosis complex))

Official abbreviation TSC
Name Tuberous sclerosis complex
OMIM ID -
Inheritance -
Individuals reported having this disease 6
Phenotype entries for this disease 6
Associated with 2 genes TSC1, TSC2
Associated tissues -
Disease features -
Remarks -


Individuals

6 entries on 1 page. Showing entries 1 - 6.
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00000234 Nur Farrah Dila Ismail et al. (2017) M Malaysia - - - - TSC - TSC1 TSC1 3 1 Nuur Athirah Binti Mohd Daud
00000235 Nur Farrah Dila Ismail et al. (2017) F Malaysia - - - - TSC - TSC1 TSC1 3 1 Nuur Athirah Binti Mohd Daud
00000236 Nur Farrah Dila Ismail et al. (2017) M Malaysia - - - - TSC - TSC2 TSC2 10 1 Nuur Athirah Binti Mohd Daud
00000237 Nur Farrah Dila Ismail et al. (2017) F Malaysia - - - - TSC - TSC2 TSC2 16 1 Nuur Athirah Binti Mohd Daud
00000743 Nur Farrah Dila Ismail et al.(2014) M Malaysia Malay - - - TSC Hypopigmented over trunk and chest, has facial angiofibroma, forehead plaque, hypomelanotic macules, cortical tuber, subependymal nodule, multiple retinal nodular hamartomas and cardiac rhabdomyoma, has cerebral white matter radial ‘migration tracts’ and multiple renal cysts. TSC2 TSC2 1 1 Nur Aisyah Athirah
00000744 Nur Farrah Dila Ismail et al.(2014) F Malaysia Malay - - - TSC Cortical tuber over the left frontal lobe and multiple small subependymal nodules along both lateral ventricle walls as well as both Foramen Monroe, has left subependymal giant cell astrocytoma, multiple subependymal hamartomas, cortical, subcortical and white matters tubers. TSC2 TSC2 1 1 Nur Aisyah Athirah
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