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Query OMIM entry list
300580
CFTD2
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION 2, X-LINKED
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Genetic Phenomena
Genetic Structures
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 6-12 and X
Chromosomes, Human, X
Sex Chromosomes
X Chromosome
Chromosomes, Human, X
Database Center for Life Science
