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SLC38A8
solute carrier family 38 member 8
gene with protein product
OMIM: 615585
1 заболевание
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Disease-causing germline mutation(s) (loss of function) in
1
Foveal hypoplasia-optic nerve decussation defect-anterior segment dysgenesis syndrome
ORPHA:397618
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Редкие заболевания
SLC38A8
🧬
SLC38A8
solute carrier family 38 member 8
gene with protein product
OMIM: 615585
1 заболевание
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Disease-causing germline mutation(s) (loss of function) in
1
Foveal hypoplasia-optic nerve decussation defect-anterior segment dysgenesis syndrome
ORPHA:397618
→