dilated cardiomyopathy 1G
dilated cardiomyopathy that has material basis in mutation in the TTN gene on chromosome 2q31
Press Enter · cited answer in seconds
0 sources
dilated cardiomyopathy 1G
Summary
dilated cardiomyopathy 1G is a rare disease[1].
Key Facts
- dilated cardiomyopathy 1G's instance of is recorded as rare disease[2].
- dilated cardiomyopathy 1G's instance of is recorded as class of disease[3].
- dilated cardiomyopathy 1G's subclass of is recorded as dilated cardiomyopathy[4].
- dilated cardiomyopathy 1G's subclass of is recorded as genetic disease[5].
- dilated cardiomyopathy 1G's subclass of is recorded as monogenic disease[6].
- dilated cardiomyopathy 1G's MeSH descriptor ID is recorded as C565824[7].
- dilated cardiomyopathy 1G's OMIM ID is recorded as 604145[8].
- dilated cardiomyopathy 1G's Disease Ontology ID is recorded as DOID:0110430[9].
- dilated cardiomyopathy 1G's NCI Thesaurus ID is recorded as C182078[10].
- dilated cardiomyopathy 1G's health specialty is recorded as cardiology[11].
- dilated cardiomyopathy 1G's genetic association is recorded as TTN[12].
- dilated cardiomyopathy 1G's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110430[13].
- dilated cardiomyopathy 1G's exact match is recorded as http://identifiers.org/doid/DOID:0110430[14].
- dilated cardiomyopathy 1G's UMLS CUI is recorded as C1858763[15].
- dilated cardiomyopathy 1G's ICD-10-CM is recorded as I42.0[16].
- dilated cardiomyopathy 1G's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].
- dilated cardiomyopathy 1G's Mondo ID is recorded as MONDO_0011400[18].
- dilated cardiomyopathy 1G's UniProt disease ID is recorded as DI-00215[19].