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SCO2
synthesis of cytochrome C oxidase 2
gene with protein product
OMIM: 604272
3 заболевания
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Герминативная мутация (причина)
3
Fatal infantile cytochrome C oxidase deficiency
ORPHA:1561
→
Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect
ORPHA:521411
→
Rare isolated myopia
ORPHA:98619
→
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SCO2
🧬
SCO2
synthesis of cytochrome C oxidase 2
gene with protein product
OMIM: 604272
3 заболевания
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Герминативная мутация (причина)
3
Fatal infantile cytochrome C oxidase deficiency
ORPHA:1561
→
Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect
ORPHA:521411
→
Rare isolated myopia
ORPHA:98619
→