| Cardiovascular
|
Arrhythmogenic right ventricular dysplasia,
arterial calcification of infancy,
Brugada syndrome,
cardiac transplant rejection,
cardiomyopathy with myopathy due to COX deficiency,
cardiomyopathy-diabetes-deafness complex,
cardiomyopathy-hypogonadism-metabolic anomalies complex,
cardiomyopathy-renal anomalies,
chronic tachycardia,
coronary artery disease,
endomyocardial fibrosis,
eosinophilic endomyocardial disease,
facio-cardio-musculo-skeletal syndrome,
giant cell myocarditis,
hypertension,
Keshan disease,
left ventricular noncompaction,
Loeffler endocarditis,
myocarditis,
Naxos disease,
obesity-colitis-hypothyroidism-cardiac hypertrophy-developmental delay,
prolonged QT syndrome,
x-linked dilated cardiomyopathy,
x-linked fatal infantile cardiomyopathy
|
| Chemical / poisoning
|
Arsenic,
cobalt,
endothall,
ethanol,
lead,
thallium,
allylamine,
carbon monoxide,
toxic mushrooms
|
| Dermatologic
|
Familial cutaneous collagenoma,
lentiginosis,
dermatomyositis,
Carvajal-Huerta syndrome,
Hand-Schuller-Christian syndrome,
McLeod syndrome,
multiple lentigines syndrome,
Naxos disease,
pityriasis lichenoides et varioliformis acuta (PLEVA),
Refsum disease
|
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5-fluorouracil,
aclarubicin,
actinomycin D,
alemtuzumab,
amrubicin,
bleomycin,
certolizumab pegol,
cisplatin,
clozapine,
cyclophosphamide,
dasatinib,
daunorubicin,
disopyramide,
doxorubicin,
epirubicin,
fenfluramine,
hydralazine,
idarubicin,
imatinib,
interferon-alfa,
mitoxantrone,
paclitaxel,
paracetamol,
pirarubicin,
pixantrone,
streptomycin,
sunitinib,
tacrolimus,
trastuzumab,
tricyclic anti-depressant abuse,
valrubicin,
|
| Ear Nose Throat
|
No underlying causes
|
| Endocrine
|
Acromegaly, Cushing's Disease, Diabetes Mellitus, Hyperparathyroidism, Hyperthyroidism, Hypothyroidism, Pheochromocytoma, Pituitary tumor (growth hormone secreting), Cardiomyopathy - diabetes - deafness, Cardiomyopathy -- hypogonadism -- metabolic anomalies complex, Obesity -- colitis -- hypothyroidism -- cardiac hypertrophy -- developmental delay, Carcinoid syndrome
|
| Environmental
|
Heatstroke, Hypothermia, Lightening strike
|
| Gastroenterologic
|
Hemochromatosis, Hepatitis, Obesity -- colitis -- hypothyroidism -- cardiac hypertrophy -- developmental delay complex, Whipple's Disease
|
| Genetic
|
Alpers Syndrome, Familial cardiomyopathy, Hutchinson-Gilford progeria syndrome, Noonan syndrome, Sarcoglycanopathy, X-linked - fatal infantile Cardiomyopathy, Friedrich's Ataxia, Brugada syndrome
|
| Hematologic
|
Cardiomyopathy -- spherocytosis
|
| Iatrogenic
|
No underlying causes
|
| Infectious Disease
|
Bacteria:
Beta-hemolytic streptococci, Borrelia burgdorferi, Brucella, Diptheria, Enterococci
, Leptospirosis, Lyme Disease, Pertussis, Psittacosis, Q Fever, Rocky Mountain Spotted Fever, Staphylococcus, Syphilis, Tetanus, Tuberculosis, Typhoid Fever, Rheumatic Fever
Virus:
Adenovirus, Arbovirus, Coxsackie virus A, Coxsackie virus B1-B5, Cytomegalovirus (CMV), ECHO virus (EnteroCytopathogenic Human Orphan viruses), Epstein-Barr Virus (EBV), Flavivirus, HIV, Influenza, Measles, Mumps,Oral candidiasis, Polio, Rabies, Varicella-zoster virus
Fungi:
Aspergillosis, Blastomycosis, Coccidioidomycosis, Cryptococcosis, Histoplasmosis
Parasites:
African Sleeping sickness, Amebiasis, Ascariasis, Chagas disease, Cysticercosis, Filariasis, Leishmaniasis, Loeffler endocarditis, Malaria, Sarcosporidiosis, Schistosomiasis, Toxoplasmosis, Trichinosis
|
| Musculoskeletal / Ortho
|
Dermatomyositis, Arthrogryposis due to muscular dystrophy, Duchenne muscular dystrophy, Emery-Dreifuss muscular dystrophy, Limb girdle muscular dystrophy, Mitochondrial myopathy, Muscular Dystrophy, Myotonic dystrophy, Recessive type Metaphyseal chondrodysplasia, Kearns-Sayre Syndrome, Cardiomyopathy with myopathy due to COX deficency, Facio-cardio-musculo-skeletal syndrome, Hand-Schuller-Christian Syndrome
|
| Neurologic
|
Friedrich's Ataxia, Kearns-Sayre Syndrome, Whipple's Disease, Alpers Syndrome, Hand-Schuller-Christian Syndrome, MELAS
|
| Nutritional / Metabolic
|
3-methylglutaconic aciduria type 4, Beri-Beri (thiamine or vitamin B1), Carbohydrate deficient glycoprotein syndrome type 1a, Carnitine deficiency, Carnitine palmitoyltransferase 2 deficiency, Carnitine transporter deficiency, Coenzyme Q 10 (CoQ10) deficiency, Coenzyme Q cytochrome c reductase deficiency, Congenital disorder of glycosylation, Cytochrome C Oxidase deficiency, Fabry's Disease, Gangliosidosis, Gaucher's Disease, Glutaric acidemia type 2, Glycogen storage diseases, Gout, Hunter's Syndrome, Hurler's Syndrome, Keshan disease, Kwashiorkor, Malonic aciduria, MELAS, Neimann-Pick Disease, Niacin deficiency, Oxalosis, Porphyria, Refsum's disease, scurvy, Triosephosphate isomerase deficiency, Vitamin B deficiency, Vitamin D overdose , Hemochromatosis
|
| Obstetric/Gynecologic
|
Peripartum cardiomyopathy
|
| Oncologic
|
Angioma, Myxomas, Pituitary tumour (growth hormone secreting), Rhabdomyoma, Sarcoma, Leukemia, WAGR Syndrome, Carcinoid syndrome
|
| Opthalmologic
|
Hand-Schuller-Christian Syndrome, Microphthalmia, syndromic 7, Myotonic dystrophy, WAGR Syndrome
|
| Overdose / Toxicity
|
No underlying causes
|
| Psychiatric
|
Takotsubo cardiomyopathy
|
| Pulmonary
|
No underlying causes
|
| Renal / Electrolyte
|
Electrolyte imbalance, Hypocalcemia, Hypokalemia, Hypomagnesemia, Uremia, WAGR Syndrome, MELAS
|
| Rheum / Immune / Allergy
|
Polyarteritis nodosa, Rheumatoid Arthritis, Sarcoidosis, Scleroderma, Systemic Lupus Erythematosus, Kawasaki's Disease, Gout
|
| Sexual
|
No underlying causes
|
| Trauma
|
Trauma
|
| Urologic
|
No underlying causes
|
| Dental
|
No underlying causes
|
| Miscellaneous
|
Cocaine abuse, Alcoholism, Amyloidosis, Electric shock, Idiopathic dilated cardiomyopathy, Immunoglobulinic amyloidosis, Irradiation, Mitochondrial trifunctional protein deficiency, Obesity, physically and physiologically stress induced (tako-tsubo syndrome or "broken heart syndrome"), Toxic mushrooms -- cyclopeptides
|