Mondo Disease Ontology
6020 terms(s) returned
| Term Type: | Record: 2151 to 2200 of 6020 Records | Page: 44 of 121, First Previous Next Last | Show Records Per Page |
- cardiomyopathy, domestic cat
- cardiomyopathy, familial hypertrophic 27
- cardiomyopathy, familial hypertrophic, 23, with or without ventricular noncompaction
- cardiomyopathy, familial hypertrophic, 28
- cardiomyopathy, familial hypertrophic, 29, with polyglucosan bodies
- cardiomyopathy, familial hypertrophic, 30, atrial
- cardiomyopathy, familial hypertrophic, 31
- cardiomyopathy, familial hypertrophic, 4, susceptibility to
- cardiomyopathy, familial restrictive, 1
- cardiomyopathy, familial restrictive, 2
- cardiomyopathy, familial restrictive, 3
- cardiomyopathy, familial restrictive, 5
- cardiomyopathy, familial restrictive, 6
- cardiomyopathy, fatal fetal, due to myocardial calcification
- cardiomyopathy, goat
- cardiomyopathy, golden hamster
- cardiomyopathy, hedgehogs
- cardiomyopathy, infantile hypertrophic
- cardiomyopathy, non-human animal
- cardiomyopathy, salmonids
- cardiomyopathy-cataract-hip spine disease syndrome
- cardiomyopathy-hypotonia-lactic acidosis syndrome
- cardiopharyngeal field
- cardioprotective agent
- cardiospondylocarpofacial syndrome
- cardiotonic drug
- cardiovascular agent therapy
- cardiovascular cancer
- cardiovascular disorder
- cardiovascular disorder, non-human animal
- cardiovascular drug
- cardiovascular neoplasm
- cardiovascular organ benign neoplasm
- cardiovascular syphilis
- cardiovascular system
- cardiovascular system elastic tissue
- cardiovascular system endothelium
- cardiovascular-kidney-metabolic syndrome
- cardiovirus infectious disease
- cargo receptor activity
- carnitine O-acetyltransferase activity
- carnitine O-acyltransferase activity
- carnitine acetyltransferase deficiency
- carnitine deficiency, myopathic
- carnitine palmitoyl transferase 1A deficiency
- carnitine palmitoyl transferase II deficiency, myopathic form
- carnitine palmitoyl transferase II deficiency, neonatal form
- carnitine palmitoyl transferase II deficiency, severe infantile form
- carnitine palmitoyl transferase deficiency
- carnitine palmitoyltransferase II deficiency
