dilated cardiomyopathy 1X
dilated cardiomyopathy that has material basis in mutation in the FKTN gene on chromosome 9q31
Press Enter · cited answer in seconds
0 sources
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's subclass of is recorded as dilated cardiomyopathy[4].
- dilated cardiomyopathy 1X's subclass of is recorded as genetic disease[5].
- dilated cardiomyopathy 1X's subclass of is recorded as autosomal recessive disease[6].
- dilated cardiomyopathy 1X's MeSH descriptor ID is recorded as C566907[7].
- dilated cardiomyopathy 1X's OMIM ID is recorded as 611615[8].
- dilated cardiomyopathy 1X's Disease Ontology ID is recorded as DOID:0110444[9].
- dilated cardiomyopathy 1X's health specialty is recorded as cardiology[10].
- dilated cardiomyopathy 1X's genetic association is recorded as FKTN[11].
- dilated cardiomyopathy 1X's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110444[12].
- dilated cardiomyopathy 1X's exact match is recorded as http://identifiers.org/doid/DOID:0110444[13].
- dilated cardiomyopathy 1X's UMLS CUI is recorded as C1969024[14].
- dilated cardiomyopathy 1X's ICD-10-CM is recorded as I42.0[15].
- dilated cardiomyopathy 1X's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
- dilated cardiomyopathy 1X's Mondo ID is recorded as MONDO_0012704[17].
- dilated cardiomyopathy 1X's UniProt disease ID is recorded as DI-00227[18].