dilated cardiomyopathy 1X
dilated cardiomyopathy that has material basis in mutation in the FKTN gene on chromosome 9q31
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dilated cardiomyopathy 1X
Summary
dilated cardiomyopathy 1X is a rare disease[1].
Key Facts
- dilated cardiomyopathy 1X's instance of is recorded as rare disease[2].
- dilated cardiomyopathy 1X's instance of is recorded as class of disease[3].
- dilated cardiomyopathy 1X is a type of dilated cardiomyopathy[4].
- dilated cardiomyopathy 1X is a type of genetic disease[5].
- dilated cardiomyopathy 1X is a type of autosomal recessive disease[6].
- dilated cardiomyopathy 1X's health specialty is recorded as cardiology[7].
- dilated cardiomyopathy 1X's genetic association is recorded as FKTN[8].
- dilated cardiomyopathy 1X's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110444[9].
- dilated cardiomyopathy 1X's exact match is recorded as http://identifiers.org/doid/DOID:0110444[10].
- dilated cardiomyopathy 1X's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].