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SLC25A26
solute carrier family 25 member 26
gene with protein product
OMIM: 611037
1 заболевание
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Disease-causing germline mutation(s) (loss of function) in
1
Neonatal severe cardiopulmonary failure due to mitochondrial methylation defect
ORPHA:466784
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Редкие заболевания
SLC25A26
🧬
SLC25A26
solute carrier family 25 member 26
gene with protein product
OMIM: 611037
1 заболевание
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Disease-causing germline mutation(s) (loss of function) in
1
Neonatal severe cardiopulmonary failure due to mitochondrial methylation defect
ORPHA:466784
→