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MED13L
mediator complex subunit 13L
gene with protein product
OMIM: 608771
2 заболевания
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Основной фактор предрасположенности
1
Isolated congenitally uncorrected transposition of the great arteries
ORPHA:216718
→
Disease-causing germline mutation(s) (loss of function) in
1
Developmental delay-facial dysmorphism syndrome due to MED13L deficiency
ORPHA:369891
→
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Редкие заболевания
MED13L
🧬
MED13L
mediator complex subunit 13L
gene with protein product
OMIM: 608771
2 заболевания
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Основной фактор предрасположенности
1
Isolated congenitally uncorrected transposition of the great arteries
ORPHA:216718
→
Disease-causing germline mutation(s) (loss of function) in
1
Developmental delay-facial dysmorphism syndrome due to MED13L deficiency
ORPHA:369891
→