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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
dilated cardiomyopathy +     
monogenic disease +     
3-methylglutaconic aciduria type 5  
Alport syndrome +   
anterior segment dysgenesis +   
autosomal genetic disease +   
Bartter disease +   
basal laminar drusen  
Brugada syndrome +   
Camurati-Engelmann disease +   
Cardiac Conduction Disease with or without Dilated Cardiomyopathy  
cardiofaciocutaneous syndrome +   
Carvajal syndrome +   
cataract +   
catecholaminergic polymorphic ventricular tachycardia +   
catecholaminergic polymorphic ventricular tachycardia 1  
chondrodysplasia punctata +   
ciliopathy +   
cone-rod dystrophy +   
Cornelia de Lange syndrome +   
corticosteroid-binding globulin deficiency  
dilated cardiomyopathy 1A  
dilated cardiomyopathy 1AA  
dilated cardiomyopathy 1B  
dilated cardiomyopathy 1BB  
dilated cardiomyopathy 1C  
dilated cardiomyopathy 1CC  
dilated cardiomyopathy 1D  
dilated cardiomyopathy 1DD  
dilated cardiomyopathy 1E  
dilated cardiomyopathy 1EE  
dilated cardiomyopathy 1FF  
dilated cardiomyopathy 1G  
dilated cardiomyopathy 1GG  
dilated cardiomyopathy 1H  
dilated cardiomyopathy 1HH  
dilated cardiomyopathy 1I  
dilated cardiomyopathy 1II  
dilated cardiomyopathy 1J  
dilated cardiomyopathy 1JJ  
dilated cardiomyopathy 1K 
dilated cardiomyopathy 1KK  
dilated cardiomyopathy 1L  
dilated cardiomyopathy 1M  
dilated cardiomyopathy 1NN  
dilated cardiomyopathy 1O  
Dilated Cardiomyopathy 1OO  
dilated cardiomyopathy 1P  
dilated cardiomyopathy 1Q 
dilated cardiomyopathy 1R  
dilated cardiomyopathy 1S  
dilated cardiomyopathy 1T  
dilated cardiomyopathy 1U  
dilated cardiomyopathy 1V  
dilated cardiomyopathy 1W  
A dilated cardiomyopathy that has_material_basis_in mutation in the VCL gene on chromosome 10q22.2. (DO)
dilated cardiomyopathy 1X  
dilated cardiomyopathy 1Y  
dilated cardiomyopathy 1Z  
dilated cardiomyopathy 2A  
dilated cardiomyopathy 2B  
dilated cardiomyopathy 2C  
dilated cardiomyopathy 2D  
dilated cardiomyopathy 2E  
dilated cardiomyopathy 2F  
dilated cardiomyopathy 2G  
Dilated Cardiomyopathy 2H  
Dilated Cardiomyopathy 2I  
Dilated Cardiomyopathy 2J  
Dilated Cardiomyopathy 3A 
Dilated Cardiomyopathy with Left Ventricular Noncompaction +   
Dilated Cardiomyopathy, Right Ventricular 
dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome  
erythrokeratodermia variabilis +   
familial hemophagocytic lymphohistiocytosis 5  
familial nephrotic syndrome +   
Fanconi anemia complementation group F  
Fanconi anemia complementation group G  
Fanconi anemia complementation group J  
Fanconi anemia complementation group N  
fetal akinesia deformation sequence syndrome +   
gene duplication disease +   
hereditary combined deficiency of vitamin K-dependent clotting factors +   
hypertrophic cardiomyopathy 25  
hypochondrogenesis  
infantile histiocytoid cardiomyopathy  
inflammatory bowel disease 1  
inflammatory bowel disease 10  
inflammatory bowel disease 11 
inflammatory bowel disease 12  
inflammatory bowel disease 13  
inflammatory bowel disease 14  
inflammatory bowel disease 15 
inflammatory bowel disease 16  
inflammatory bowel disease 17  
inflammatory bowel disease 18 
inflammatory bowel disease 19  
inflammatory bowel disease 2 
inflammatory bowel disease 20 
inflammatory bowel disease 22 
inflammatory bowel disease 23 
inflammatory bowel disease 24 
inflammatory bowel disease 26 
inflammatory bowel disease 27 
inflammatory bowel disease 4 
inflammatory bowel disease 5  
inflammatory bowel disease 6 
inflammatory bowel disease 7 
inflammatory bowel disease 8 
inflammatory bowel disease 9 
isolated microphthalmia 4  
Krasnow Qazi Syndrome 
lambda 5 deficiency 
Leber congenital amaurosis 10  
Leber congenital amaurosis 3  
Leber congenital amaurosis 7  
LONG-OLSEN-DISTELMAIER SYNDROME  
multiple epiphyseal dysplasia due to collagen 9 anomaly +   
Noonan syndrome +   
osteogenesis imperfecta type 14  
osteogenesis imperfecta type 6  
peripartum cardiomyopathy  
posterior polymorphous corneal dystrophy 3  
postural orthostatic tachycardia syndrome 
primary congenital glaucoma +   
Ritscher-Schinzel syndrome +   
schizophrenia 13 
schizophrenia 14 
schizophrenia 16 
schizophrenia 18  
schizophrenia 9  
SHOX-related short stature  
Uhl Anomaly 
Winship Viljoen Leary Syndrome 
X-linked dilated cardiomyopathy +   
X-linked monogenic disease +   
Y-linked monogenic disease +   

Synonyms
Exact Synonyms: CMD1W
Broad Synonyms: VCL-RELATED CONDITION
Primary IDs: MESH:C566954
Alternate IDs: OMIM:611407
Xrefs: NCI:C187983
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/11815424 "DO" "DO"

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