Fever, and Myocardial infarction

Diseases related with Fever and Myocardial infarction

In the following list you will find some of the most common rare diseases related to Fever and Myocardial infarction that can help you solving undiagnosed cases.

Top matches:

Budd-Chiari syndrome (BCS) is caused by obstruction of hepatic venous outflow involving either the hepatic veins or the terminal segment of the inferior vena cava.

Related symptoms:

  • Neoplasm
  • Pain
  • Hypertension
  • Hepatomegaly
  • Fever


SOURCES: MESH OMIM ORPHANET MENDELIAN

More info about BUDD-CHIARI SYNDROME

Takayasu arteritis (TAK) is a rare inflammatory large-vessel vasculitis primarily affecting the aorta and its major branches, but also other large vessels, causing stenosis, occlusion, or aneurysm.

TAKAYASU ARTERITIS Is also known as young female arteritis|aortic arch syndrome|pulseless disease

Related symptoms:

  • Seizures
  • Muscle weakness
  • Anemia
  • Hypertension
  • Fever


SOURCES: ORPHANET OMIM MENDELIAN

More info about TAKAYASU ARTERITIS

Lymphangioleiomyomatosis (LAM) is a multiple cystic lung disease characterized by progressive cystic destruction of the lung and lymphatic abnormalities, frequently associated with renal angiomyolipomas (AMLs). LAM occurs either sporadically or as a manifestation of tuberous sclerosis complex (TSC).

LYMPHANGIOLEIOMYOMATOSIS Is also known as lam|lymphangiomyomatosis

Related symptoms:

  • Seizures
  • Pain
  • Cognitive impairment
  • Fever
  • Optic atrophy


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about LYMPHANGIOLEIOMYOMATOSIS

Other less relevant matches:

Stevens-Johnson syndrome is a limited form of toxic epidermal necrolysis (see this term) characterized by destruction and detachment of the skin epithelium and mucous membranes involving less than 10% of the body surface area.

STEVENS-JOHNSON SYNDROME Is also known as dermatostomatitis, stevens johnson type

Related symptoms:

  • Anemia
  • Visual impairment
  • Fever
  • Fatigue
  • Dysphagia


SOURCES: MESH OMIM ORPHANET MENDELIAN

More info about STEVENS-JOHNSON SYNDROME

Familial Mediterranean fever (FMF) is an autoinflammatory disorder characterized by recurrent short episodes of fever and serositis resulting in pain in the abdomen, chest, joints and muscles.

FAMILIAL MEDITERRANEAN FEVER Is also known as benign paroxysmal peritonitis|familial paroxysmal polyserositis|benign recurrent polyserositis|polyserositis, familial paroxysmal|fmf|periodic disease|familial mediterranean fever, autosomal recessive|polyserositis, recurrent

Related symptoms:

  • Seizures
  • Pain
  • Anemia
  • Hepatomegaly
  • Fever


SOURCES: OMIM ORPHANET MENDELIAN

More info about FAMILIAL MEDITERRANEAN FEVER

High match KAWASAKI DISEASE

Kawasaki disease (KD) is a febrile, systemic, self-limiting vasculitis affecting children and characterized by inflammation in the medium sized vessels associated with coronary arterial aneurysms (CAA) that may be life threatening when untreated. KD is the most common cause of acquired heart disease in children in developed countries and is a risk factor for ischemic heart disease in adulthood.

KAWASAKI DISEASE Is also known as kd|infantile polyarteritis|mucocutaneous lymph node syndrome

Related symptoms:

  • Sensorineural hearing impairment
  • Ptosis
  • Fever
  • Fatigue
  • Edema


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about KAWASAKI DISEASE

High match CADASIL

CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy) is a hereditary cerebrovascular disorder characterized by mid-adult onset of recurrent subcortical ischemic stroke and cognitive impairment progressing to dementia in addition to migraines with aura and mood disturbances seen in about a third of patients.

CADASIL Is also known as dementia, hereditary multi-infarct type|cadasil|cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy|casil|hereditary multi-infarct dementia

Related symptoms:

  • Seizures
  • Hearing impairment
  • Ataxia
  • Sensorineural hearing impairment
  • Muscle weakness


SOURCES: OMIM ORPHANET MENDELIAN

More info about CADASIL

Fibrodysplasia ossificans progressiva (FOP) is a severely disabling heritable disorder of connective tissue characterized by congenital malformations of the great toes and progressive heterotopic ossification that forms qualitatively normal bone in characteristic extraskeletal sites.

FIBRODYSPLASIA OSSIFICANS PROGRESSIVA Is also known as stone man syndrome|fop|myositis ossificans progressiva

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Hearing impairment
  • Scoliosis


SOURCES: OMIM ORPHANET MENDELIAN

More info about FIBRODYSPLASIA OSSIFICANS PROGRESSIVA

Granulomatosis with polyangiitis is a small-vessel necrotizing vasculitis characterised by the association of inflammation of the vessel wall and peri- and extravascular granulomatosis.

GRANULOMATOSIS WITH POLYANGIITIS Is also known as wegener granulomatosis, formerly|gpa|wg, formerly

Related symptoms:

  • Seizures
  • Hearing impairment
  • Sensorineural hearing impairment
  • Pain
  • Visual impairment


SOURCES: ORPHANET OMIM MESH MENDELIAN

More info about GRANULOMATOSIS WITH POLYANGIITIS

High match BEHÇET DISEASE

Behçet's disease (BD) is a chronic, relapsing, multisystemic vasculitis characterized by mucocutaneous lesions, as well as articular, vascular, ocular and central nervous system manifestations.

BEHÇET DISEASE Is also known as bd|behcet disease

Related symptoms:

  • Seizures
  • Ataxia
  • Neoplasm
  • Pain
  • Cataract


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about BEHÇET DISEASE

Top 5 symptoms//phenotypes associated to Fever and Myocardial infarction

Symptoms // Phenotype % cases
Abdominal pain Common - Between 50% and 80% cases
Seizures Common - Between 50% and 80% cases
Pain Common - Between 50% and 80% cases
Fatigue Common - Between 50% and 80% cases
Chest pain Uncommon - Between 30% and 50% cases

Other less frequent symptoms

Patients with Fever and Myocardial infarction. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases

Gastrointestinal hemorrhage Vasculitis Arthritis Arthralgia Headache Nausea and vomiting Weight loss Diarrhea Anemia Sensorineural hearing impairment Hemoptysis Cerebral ischemia Renal insufficiency Myalgia Pancreatitis Hypertension Meningitis Migraine Pericarditis Skin rash Erythema Subcutaneous nodule Dyspnea Cranial nerve paralysis Stroke Cough Lymphadenopathy Pulmonary infiltrates Restrictive ventilatory defect Arrhythmia Hematuria Visual impairment Gangrene Abnormal myocardium morphology Inflammatory abnormality of the eye Hearing impairment Conjunctivitis Arteritis Increased inflammatory response Recurrent respiratory infections Neoplasm Proteinuria Acute hepatic failure Gastrointestinal infarctions Visual loss Retinopathy Pleuritis Elevated erythrocyte sedimentation rate Splenomegaly Dilatation Ascites Myositis Nausea Intestinal obstruction Malabsorption

Rare Symptoms - Less than 30% cases

Photophobia Venous thrombosis Orchitis Mitral regurgitation Peripheral neuropathy Hyperreflexia Respiratory insufficiency Respiratory tract infection Gait disturbance Endocarditis Dysphagia Ataxia Stiff neck Papule Pleural effusion Nephropathy Elevated C-reactive protein level Glomerulopathy Glaucoma Paresthesia Purpura Alopecia Synovitis Autoimmunity Rheumatoid arthritis Inflammation of the large intestine Leukocytosis Hepatitis Abnormal blistering of the skin Amyloidosis Behavioral abnormality Congestive heart failure Anorexia Respiratory failure Muscle weakness Sensory neuropathy Memory impairment Skin ulcer Aortic regurgitation Cholecystitis Peritonitis Varicose veins Abnormal heart valve morphology Vertigo Confusion Ascending tubular aorta aneurysm Cognitive impairment Respiratory distress Amaurosis fugax Scarring Hepatomegaly Hemiparesis Developmental regression Jaundice Elevated hepatic transaminase Hemiplegia Macule Irritability Bulbar palsy Scotoma Metaphyseal widening Cerebral hemorrhage Broad femoral neck Impaired pain sensation Optic neuropathy Abnormality of visual evoked potentials Overbite Aphasia Short 1st metacarpal Short hallux Hallux valgus Spinal rigidity Hamartoma Apathy Basal ganglia calcification Back pain Alopecia of scalp Personality changes Ankylosis Exostoses Broad neck Transient ischemic attack Global developmental delay Sarcoma Recurrent subcortical infarcts Diffuse leukoencephalopathy Focal sensory seizure Kyphosis Retinal arteriolar tortuosity Subcortical dementia Abulia Nonarteritic anterior ischemic optic neuropathy Subcutaneous hemorrhage Intellectual disability, mild Scintillating scotoma Abnormality of the skeletal system Flexion contracture Low-set ears Intellectual disability Failure to thrive Clinodactyly Mania Stroke-like episode Short thumb Widely spaced teeth Finger clinodactyly Migraine with aura Aspiration Scoliosis Abnormal vertebral morphology Limitation of joint mobility Perseveration Hypotrichosis Conductive hearing impairment Abnormality of nervous system morphology Difficulty walking Pneumonia Clinodactyly of the 5th finger Pseudobulbar paralysis Subdural hemorrhage Stridor Low-grade fever Encephalitis Uveitis Aseptic necrosis Pulmonary embolism Keratoconjunctivitis sicca Blurred vision Epiphora Acne Increased intracranial pressure Raynaud phenomenon Abnormal pyramidal sign Joint stiffness Reduced visual acuity Blindness Cataract Prostatitis Recurrent intrapulmonary hemorrhage Scleritis Pustule Arterial thrombosis Abnormal oral cavity morphology Posterior uveitis Decreased level of D-mannose in urine Epididymitis Genital ulcers Panuveitis Superficial thrombophlebitis Retrobulbar optic neuritis Iritis Iridocyclitis Anterior uveitis Recurrent aphthous stomatitis Optic neuritis Chorioretinitis Immunologic hypersensitivity Erythema nodosum Thrombophlebitis Oral ulcer Alopecia areata Stomatitis Episcleritis Ureteral stenosis Soft tissue sarcoma Abnormality of the first metatarsal bone Diplopia Epistaxis Otitis media Paralysis Hydronephrosis Proptosis Cardiomyopathy Aplasia/Hypoplasia of the phalanges of the hallux Progressive cervical vertebral spine fusion Hoarse voice Ectopic ossification in tendon tissue Ectopic ossification in ligament tissue Ectopic ossification in muscle tissue Small cervical vertebral bodies Ectopic ossification Fibrosarcoma Osteochondroma Synostosis of joints Sinusitis Glomerulonephritis Neuritis Abnormality of the nose Granulomatosis Subglottic stenosis Ocular pain Rhinorrhea Periorbital edema Nasal obstruction Recurrent corneal erosions Abnormality of the hypothalamus-pituitary axis Concave nasal ridge Chronic otitis media Angina pectoris Chronic obstructive pulmonary disease Tracheal stenosis Wheezing Petechiae Pulmonary fibrosis Diabetes insipidus Leukoencephalopathy Abnormal electroretinogram Abnormal gallbladder morphology Shock Sepsis Excessive salivation Entropion Dysuria Corneal erosion Nephritis Eosinophilia Sudden cardiac death Thrombocytopenia Esophageal stricture Chylopericardium Pulmonary lymphangiomyomatosis Cystic lung disease Ungual fibroma Retinal hamartoma Renal angiomyolipoma Bronchiolitis obliterans Abnormality of the pleura Acantholysis Abnormal urinary color Asthma Episodic fever Hyperkalemia Systemic lupus erythematosus Chronic kidney disease Nephrocalcinosis Osteoarthritis Nephrotic syndrome Stage 5 chronic kidney disease Abnormality of neutrophils Abnormality of the kidney Hepatosplenomegaly Acidosis Constipation Dyspareunia Hypokalemic metabolic alkalosis Abnormality of the urethra Shagreen patch Abnormality of the lymphatic system Gout Portal vein thrombosis Pulmonary arterial hypertension Neurological speech impairment Hypertrophic cardiomyopathy Hyperhidrosis Hepatic vein thrombosis Reduced protein C activity Budd-Chiari syndrome Esophageal varix Reduced consciousness/confusion Hypercoagulability Hepatocellular carcinoma Thromboembolism Polycythemia Portal hypertension Cirrhosis Carcinoma Psoriasiform dermatitis Abnormal aortic valve morphology Chylothorax Nephroblastoma Bronchiolitis Pneumothorax Abnormality of female internal genitalia Atelectasis Renal neoplasm Multiple renal cysts Emphysema Melanoma Abnormal pattern of respiration Lymphedema Abnormal lung morphology Abnormality of skin pigmentation Hydrocephalus Optic atrophy Hypertensive crisis Abnormal endocardium morphology Arterial stenosis Increased serum ferritin Antinuclear antibody positivity Atherosclerosis Elevated serum creatine phosphokinase Mental deterioration Facial palsy Hypoglycemia EEG abnormality Cerebral cortical atrophy Dementia Babinski sign Encephalopathy Pallor Depressivity Hypertonia Vomiting Myopathy Tremor Dysarthria Delayed speech and language development Abnormality of the eye Attention deficit hyperactivity disorder Aseptic leukocyturia Peripheral demyelination Spastic tetraparesis Recurrent pneumonia Truncal ataxia Tetraparesis Psychosis Abnormality of extrapyramidal motor function Bradykinesia Abnormality of the skin Generalized tonic-clonic seizures Urinary incontinence Brain atrophy Tetraplegia Coma Inability to walk Dysmetria Lower limb muscle weakness Abnormality of eye movement Spasticity Strawberry tongue Edema of the lower limbs Recurrent meningitis Scaling skin Hypoalbuminemia Ischemic stroke Decreased liver function Cholestasis Edema Ptosis Serositis Coronary artery atherosclerosis Azotemia Renal amyloidosis Erysipelas Congenital hypoplastic anemia Decreased circulating aldosterone level Anemia of inadequate production Oral leukoplakia Hyponatremia Interstitial pulmonary abnormality Double outlet right ventricle with subpulmonary ventricular septal defect without pulmonary stenosis Conjunctival hyperemia Abnormal emotion/affect behavior Pyuria Arthralgia/arthritis Abnormality of nail color Coronary artery aneurysm Cervical lymphadenopathy CSF pleocytosis Abnormal pericardium morphology Acute kidney injury Glossitis Abnormal oral mucosa morphology Cheilitis Recurrent pharyngitis Allergy Myocarditis Tubulointerstitial nephritis Aortic root aneurysm Hypopyon


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