dilated cardiomyopathy 1D
dilated cardiomyopathy that has material basis in mutation in the TNNT2 gene on chromosome 1q32
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dilated cardiomyopathy 1D
Summary
dilated cardiomyopathy 1D is a rare disease[1].
Key Facts
- dilated cardiomyopathy 1D's instance of is recorded as rare disease[2].
- dilated cardiomyopathy 1D's instance of is recorded as class of disease[3].
- dilated cardiomyopathy 1D's subclass of is recorded as dilated cardiomyopathy[4].
- dilated cardiomyopathy 1D's subclass of is recorded as genetic disease[5].
- dilated cardiomyopathy 1D's subclass of is recorded as autosomal dominant disease[6].
- dilated cardiomyopathy 1D's MeSH descriptor ID is recorded as C563306[7].
- dilated cardiomyopathy 1D's OMIM ID is recorded as 601494[8].
- dilated cardiomyopathy 1D's Disease Ontology ID is recorded as DOID:0110426[9].
- dilated cardiomyopathy 1D's NCI Thesaurus ID is recorded as C198599[10].
- dilated cardiomyopathy 1D's health specialty is recorded as cardiology[11].
- dilated cardiomyopathy 1D's genetic association is recorded as TNNT2[12].
- dilated cardiomyopathy 1D's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110426[13].
- dilated cardiomyopathy 1D's exact match is recorded as http://identifiers.org/doid/DOID:0110426[14].
- dilated cardiomyopathy 1D's UMLS CUI is recorded as C1832243[15].
- dilated cardiomyopathy 1D's ICD-10-CM is recorded as I42.0[16].
- dilated cardiomyopathy 1D's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].
- dilated cardiomyopathy 1D's Mondo ID is recorded as MONDO_0011095[18].
- dilated cardiomyopathy 1D's UniProt disease ID is recorded as DI-00213[19].