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MYH2
myosin heavy chain 2
gene with protein product
OMIM: 160740
2 заболевания
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Disease-causing germline mutation(s) (loss of function) in
1
Childhood-onset autosomal recessive myopathy with external ophthalmoplegia
ORPHA:363677
→
Герминативная мутация (причина)
1
Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome
ORPHA:79091
→
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Редкие заболевания
MYH2
🧬
MYH2
myosin heavy chain 2
gene with protein product
OMIM: 160740
2 заболевания
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Disease-causing germline mutation(s) (loss of function) in
1
Childhood-onset autosomal recessive myopathy with external ophthalmoplegia
ORPHA:363677
→
Герминативная мутация (причина)
1
Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome
ORPHA:79091
→