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Ontology Browser

Term:
Fatal Fetal Cardiomyopathy due to Myocardial Calcification (DOID:9005039)
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Parent Terms Term With Siblings Child Terms
calcinosis +     
cardiomyopathy +     
Fetal Death +     
alcoholic cardiomyopathy  
ARRHYTHMOGENIC CARDIOMYOPATHY WITH VARIABLE ECTODERMAL ABNORMALITIES  
Ataxia, Deafness, and Cardiomyopathy 
Atrial Dilation and Standstill +   
autosomal recessive limb-girdle muscular dystrophy type 2D  
Axonal Encephalopathy with Necrotizing Myopathy, Cardiomyopathy, and Cataracts 
basal ganglia calcification +   
Berry Aneurysm, Cirrhosis, Pulmonary Emphysema, and Cerebral Calcification 
Calcific Aortic Disease with Immunologic Abnormalities, Familial 
Calcification of Aortic Valve +   
calciphylaxis 
Cardiomyopathy Associated with Myopathy and Sudden Death 
Cardiomyopathy Hypogonadism Collagenoma Syndrome 
Cardioneuromyopathy with Hyaline Masses and Nemaline Rods 
Cerebroretinal Microangiopathy with Calcifications and Cysts +   
Chagas Cardiomyopathy  
Choroid Plexus Calcification with Mental Retardation 
Cole Disease  
congenital myopathy 5  
CREST syndrome  
Danon disease  
Diabetic Cardiomyopathies  
diffuse idiopathic skeletal hyperostosis +   
Encephalopathy with Intracranial Calcification, Growth Hormone Deficiency, Microcephaly, and Retinal Degeneration 
endocardial fibroelastosis +   
endomyocardial fibrosis  
Epilepsy, Occipital Calcifications 
extrinsic cardiomyopathy +   
Facial Dysmorphism, Selective Tooth Agenesis, and Choroid Calcification 
Familial Cardiac Lipidosis 
Fatal Fetal Cardiomyopathy due to Myocardial Calcification 
Fetal Resorption  
Greenberg dysplasia  
Hemorrhagic Destruction of the Brain, Subependymal Calcification, and Cataracts  
hereditary arterial and articular multiple calcification syndrome +   
hyperphosphatemic familial tumoral calcinosis +   
Hypertaurinuric Cardiomyopathy  
intrinsic cardiomyopathy +   
Kearns-Sayre syndrome  
Keshan disease  
Keutel Syndrome  
Labrune Syndrome  
linear skin defects with multiple congenital anomalies 3  
Medial Coronary Sclerosis of Infancy  
Mitochondrial Cardiomyopathy  
mitochondrial DNA depletion syndrome 12a  
mitochondrial DNA depletion syndrome 12b  
Muscular Dystrophy, Cardiac Type 
Myocardial Reperfusion Injury  
myocarditis +   
myofibrillar myopathy 2  
nephrocalcinosis +   
Nephrogenic Diabetes Insipidus with Mental Retardation and Intracerebral Calcification 
neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities  
Neurodevelopmental Disorder with Seizures, Microcephaly, and Brain Abnormalities  
nonischemic cardiomyopathy 
normophosphatemic familial tumoral calcinosis  
Ossified Ear Cartilages 
Piepkorn Karp Hickok syndrome 
Primrose Syndrome  
Pseudo-TORCH Syndrome +   
pulmonary alveolar microlithiasis  
Raine Syndrome  
Rajab Interstitial Lung Disease with Brain Calcifications +   
Rambaud Galian Syndrome 
Renal Hypophosphatemia with Intracerebral Calcifications 
Roifman Syndrome  
Schofer Beetz Bohl Syndrome 
Sengers syndrome  
Spondylomegaepiphyseal Dysplasia with Upper Limb Mesomelia, Punctate Calcifications, and Deafness 
Stillbirth 
Storm Syndrome 
systemic primary carnitine deficiency disease  
Thymic Aplasia with Fetal Death 
Tropical Calcific Pancreatitis  
Uruguay faciocardiomusculoskeletal syndrome  
Vascular Calcification +   
Whyte Murphy Fallon Sly syndrome 

Synonyms
Exact Synonyms: Myocardial calcifications resulting in intrauterine fetal death
Primary IDs: MESH:C543241
Alternate IDs: MIM:300829

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