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Ontology Browser

Term:
infantile histiocytoid cardiomyopathy (DOID:0080198)
Annotations: Rat: (3) Mouse: (3) Human: (3) Chinchilla: (2) Bonobo: (2) Dog: (3) Squirrel: (2) Pig: (3)
Parent Terms Term With Siblings Child Terms
cardiomyopathy +     
monogenic disease +     
alcoholic cardiomyopathy  
Alport syndrome +   
amyotrophic lateral sclerosis +   
arrhythmogenic right ventricular cardiomyopathy +   
Ataxia, Deafness, and Cardiomyopathy 
Atrial Dilation and Standstill +   
autosomal genetic disease +   
autosomal recessive limb-girdle muscular dystrophy type 2D  
Axonal Encephalopathy with Necrotizing Myopathy, Cardiomyopathy, and Cataracts 
Bartter disease +   
basal laminar drusen  
Brugada syndrome +   
Camurati-Engelmann disease +   
cardiofaciocutaneous syndrome +   
Cardiomyopathy Associated with Myopathy and Sudden Death 
Cardiomyopathy Hypogonadism Collagenoma Syndrome 
Cardioneuromyopathy with Hyaline Masses and Nemaline Rods 
cataract +   
catecholaminergic polymorphic ventricular tachycardia +   
Cayman type cerebellar ataxia  
Chagas Cardiomyopathy  
chondrodysplasia punctata +   
ciliopathy +   
cone-rod dystrophy +   
Cornelia de Lange syndrome +   
corticosteroid-binding globulin deficiency  
Danon disease  
Diabetic Cardiomyopathies  
dilated cardiomyopathy +   
dilated cardiomyopathy 1BB  
dilated cardiomyopathy 1EE  
dilated cardiomyopathy 1FF  
dilated cardiomyopathy 1G  
dilated cardiomyopathy 1GG  
dilated cardiomyopathy 1H  
dilated cardiomyopathy 1I  
dilated cardiomyopathy 1J  
dilated cardiomyopathy 1K 
dilated cardiomyopathy 1L  
dilated cardiomyopathy 1M  
dilated cardiomyopathy 1O  
dilated cardiomyopathy 1P  
dilated cardiomyopathy 1Q 
dilated cardiomyopathy 1T  
dilated cardiomyopathy 1W  
dilated cardiomyopathy 1Z  
Early-Onset Myopathy with Fatal Cardiomyopathy  
endocardial fibroelastosis +   
endomyocardial fibrosis  
erythrokeratodermia variabilis +   
extrinsic cardiomyopathy +   
Familial Cardiac Lipidosis 
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  
Fatal Fetal Cardiomyopathy due to Myocardial Calcification 
Hypertaurinuric Cardiomyopathy 
hypertrophic cardiomyopathy +   
hypochondrogenesis  
infantile histiocytoid cardiomyopathy  
An intrinsic cardiomyopathy characterized by the presence of characteristic pale granular foamy histiocyte-like cells within the myocardium and has_material_basis_in a mutation in the gene encoding mitochondrial cytochrome b. (DO)
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 
intrinsic cardiomyopathy +   
isolated microphthalmia 4  
Kearns-Sayre syndrome  
Keshan disease  
lambda 5 deficiency 
Leber congenital amaurosis 10  
Leber congenital amaurosis 3  
Leber congenital amaurosis 7  
left ventricular noncompaction +   
Linear Skin Defects with Multiple Congenital Anomalies 3  
long QT syndrome +   
Mitochondrial Cardiomyopathy  
mitochondrial DNA depletion syndrome 12a  
mitochondrial DNA depletion syndrome 12b  
multiple epiphyseal dysplasia due to collagen 9 anomaly 
multiple pterygium syndrome +   
Muscular Dystrophy, Cardiac Type 
Myocardial Reperfusion Injury  
myocarditis +   
myofibrillar myopathy 2  
Noonan syndrome +   
Opitz-GBBB syndrome +   
osteogenesis imperfecta type 14  
osteogenesis imperfecta type 6  
posterior polymorphous corneal dystrophy 3  
postural orthostatic tachycardia syndrome  
primary congenital glaucoma +   
restrictive cardiomyopathy +   
Ritscher-Schinzel syndrome +   
Roifman Syndrome  
schizophrenia 13 
schizophrenia 14 
schizophrenia 16  
schizophrenia 18  
schizophrenia 9  
Sengers syndrome  
systemic primary carnitine deficiency disease  
Uruguay Faciocardiomusculoskeletal Syndrome  
X-linked monogenic disease +   
Y-linked monogenic disease +   

Synonyms
Exact Synonyms: Infantile xanthomatous cardiomyopathy ;   foamy myocardial transformation of infancy ;   focal lipid cardiomyopathy ;   oncocytic cardiomyopathy
Primary IDs: MESH:C535584
Alternate IDs: OMIM:500000 ;   RDO:0000796
Xrefs: GARD:9511
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/10960495

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.