familial dilated cardiomyopathy
A a genetic form of heart disease that occurs when heart (cardiac) muscle becomes thin and weakened in at least one chamber of the heart, causing the open area of the chamber to become enlarged (dilated). As a result, the heart is unable to pump blood as efficiently as usual. To compensate, the heart attempts to increase the amount of blood being pumped through the heart, leading to further thinning and weakening of the cardiac muscle. Over time, this condition results in heart failure. [ https://ghr.nlm.nih.gov/condition/familial-dilated-cardiomyopathy ]
Term info
- MESH:C536231 (Orphanet:217607/e)
- GARD:0000221 (MONDO:equivalentTo)
- Orphanet:217607 (MONDO:equivalentTo)
- UMLS:C0340427 (Orphanet:217607/e)
- OMIMPS:115200 (MONDO:equivalentTo)
- GARD:0002905 (MONDO:equivalentTo)
disease_grouping, ordo_group_of_disorders
Editor note: unsure if GARD is familial form
A a genetic form of heart disease that occurs when heart (cardiac) muscle becomes thin and weakened in at least one chamber of the heart, causing the open area of the chamber to become enlarged (dilated). As a result, the heart is unable to pump blood as efficiently as usual. To compensate, the heart attempts to increase the amount of blood being pumped through the heart, leading to further thinning and weakening of the cardiac muscle. Over time, this condition results in heart failure.
http://linkedlifedata.com/resource/umls/id/C0340427, http://identifiers.org/mesh/C536231, http://purl.obolibrary.org/obo/Orphanet_217607, https://omim.org/phenotypicSeries/PS115200
hereditary dilated cardiomyopathy
dilated cardiomyopathy, familial, idiopathic dilated cardiomyopathy, hypokinetic dilated cardiomyopathy, familial, DCM
MONDO:0016333