| 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
|
| Drug Side Effect
|
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,
amyloidosis,
carcinoid syndrome,
cardiomyopathy-diabetes-deafness complex,
cardiomyopathy-hypogonadism-metabolic anomalies complex,
celiac disease,
cushing syndrome,
diabetes Mellitus,
gout,
hemochromatosis,
hyperparathyroidism,
hyperthyroidism,
hypothyroidism,
obesity-colitis-hypothyroidism-cardiac hypertrophy developmental delay,
paraneoplastic syndromes,
pheochromocytoma,
pituitary tumor (growth hormone secreting),
WAGR syndrome,
Whipple's disease
|
| Environmental
|
Heatstroke, hypothermia, lightening strike, radiation
|
| Gastroenterologic
|
Hemochromatosis, obesity-colitis-hypothyroidism-cardiac hypertrophy-developmental delay complex, Whipple's Disease
|
| Genetic
|
Alpers' syndrome,
Brugada syndrome,
Carvajal-Huerta syndrome,
chromosome 11, partial deletion,
congenital disorders of glycosylation type 1a,
congenital generalized lipodystrophy type 2,
Costello syndrome,
desmin myopathy,
Emery-Dreifuss muscular dystrophy,
facio-cardio-musculo-skeletal syndrome,
familial cardiomyopathy,
Friedreich's ataxia,
hereditary spherocytosis,
Hurler syndrome,
Hutchinson-Gilford progeria syndrome,
hypertrichotic osteochondrodysplasia (Cantu syndrome),
Keshan disease,
Laing distal myopathy,
LAMA2-related muscular dystrophy,
metaphyseal chondrodysplasia, recessive type,
mitochondrial trifunctional protein deficiency,
multiple lentigines syndrome,
muscular dystrophy,
Naxos disease,
Noonan syndrome,
porphyria,
prolonged QT syndrome,
pseudoxanthoma elasticum,
Refsum disease,
Salih myopathy,
sarcoglycanopathy,
syndromic microphthalmia type 7,
WAGR syndrome,
x-linked dilated cardiomyopathy,
x-linked fatal infantile cardiomyopathy,
Yunis-Varon syndrome
|
| Hematologic
|
Hereditary spherocytosis
|
| Iatrogenic
|
No underlying causes
|
| Infectious Disease
|
Bacteria:
Beta-hemolytic streptococci,
brucella,
diptheria,
enterococci
leptospirosis,
Lyme disease,
pertussis,
psittacosis,
Q fever,
rheumatic fever
rocky mountain spotted fever,
staphylococcus,
syphilis,
tetanus,
tuberculosis,
typhoid 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,
poliomyelitis,
rabies,
varicella-zoster virus
Fungi:
Aspergillosis,
blastomycosis,
coccidioidomycosis,
cryptococcosis,
histoplasmosis
Parasites:
African trypanosomiasis,
ascariasis,
Chagas disease,
cysticercosis,
filariasis,
leishmaniasis,
loeffler endocarditis,
malaria,
sarcosporidiosis,
schistosomiasis,
toxoplasmosis,
trichinosis
|
| Musculoskeletal / Ortho
|
Arthrogryposis due to muscular dystrophy,
cardiomyopathy with myopathy due to cox deficency,
dermatomyositis,
duchenne muscular dystrophy,
Emery-Dreifuss muscular dystrophy,
facio-cardio-musculo-skeletal syndrome,
Hand-Schuller-Christian Syndrome,
Kearns-Sayre syndrome,
metaphyseal chondrodysplasia, recessive type,
mitochondrial myopathy,
muscular dystrophy,
myotonic dystrophy
|
| Neurologic
|
Alpers' syndrome,
Friedreich's ataxia,
Hand-Schuller-Christian Syndrome,
Kearns-Sayre syndrome,
MELAS syndrome
Whipple's disease
|
| Nutritional / Metabolic
|
3-methylglutaconic aciduria type 4,
beriberi (thiamine or vitamin B1),
carbohydrate deficient glycoprotein syndrome type 1a,
carnitine deficiency,
coenzyme Q10 (CoQ10) deficiency,
coenzyme Q cytochrome c reductase deficiency,
congenital disorder of glycosylation,
cytochrome C Oxidase deficiency,
d-2-hydroxyglutarate dehydrogenase deficiency,
Fabry disease,
fatty infiltration of the heart,
gangliosidosis,
Gaucher's disease,
glutaric acidemia type 2,
gout,
hemochromatosis,
Hunter syndrome,
Hurler syndrome,
isobutyryl-Coa dehydrogenase deficiency,
Keshan disease,
kwashiorkor,
long-chain Acyl Coa dehydrogenase deficiency,
malonic aciduria,
malonyl-Coa decarboxylase deficiency,
MELAS syndrome,
mitochondrial trifunctional protein deficiency,
mucopolysaccharidoses,
Neimann-Pick disease,
niacin deficiency,
oxalosis,
paraneoplastic syndromes,
Pompe disease,
porphyria,
Refsum disease,
respiratory chain complex I deficiency,
s-adenosylhomocysteine hydrolase deficiency,
scurvy,
selenium deficiency,
subacute necrotising encephalomyelopathy (Leigh's disease),
triosephosphate isomerase deficiency,
Uremia
vitamin B deficiency,
vitamin D overdose
|
| 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
|
Alcohol,
cobalt poisoning,
cocaine abuse,
oxalosis,
paracetamol,
tricyclic antidepressant abuse,
vitamin D overdose
|
| Psychiatric
|
Takotsubo cardiomyopathy
|
| Pulmonary
|
No underlying causes
|
| Renal / Electrolyte
|
Hypocalcemia,
hypokalemia,
hypomagnesemia,
uremia,
WAGR syndrome,
MELAS syndrome
|
| Rheum / Immune / Allergy
|
Gout,
Kawasaki disease,
polyarteritis nodosa,
rheumatoid arthritis,
systemic sclerosis,
scleroderma,
systemic lupus erythematosus
|
| Sexual
|
No underlying causes
|
| Trauma
|
No underlying causes
|
| Urologic
|
No underlying causes
|
| Dental
|
No underlying causes
|
| Miscellaneous
|
Black widow spider bite,
cardiac transplant rejection,
idiopathic dilated cardiomyopathy,
mitochondrial trifunctional protein deficiency,
obesity,
obstructive sleep apnea,
stress-induced cardiomyopathy
|