Autoimmunity, and Myocardial infarction

Diseases related with Autoimmunity and Myocardial infarction

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


Top matches:

Medium match SNEDDON SYNDROME


Sneddon's syndrome (SS) is a rare non-inflammatory thrombotic vasculopathy characterized by the combination of cerebrovascular disease with livedo racemosa.

SNEDDON SYNDROME Is also known as livedo reticularis-cerebrovascular accident syndrome|livedo racemosa-cerebrovascular accident syndrome|livedo reticularis and cerebrovascular accidents|ehrmann-sneddon syndrome

Related symptoms:

  • Seizures
  • Muscle weakness
  • Pain
  • Visual impairment
  • Motor delay


SOURCES: OMIM MESH ORPHANET MENDELIAN

More info about SNEDDON SYNDROME

Medium match FAMILIAL MEDITERRANEAN FEVER


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

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Other less relevant matches:

Medium match WOODHOUSE-SAKATI SYNDROME


Woodhouse-Sakati syndrome is a multisystemic disorder characterized by hypogonadism, alopecia, diabetes mellitus, intellectual deficit and extrapyramidal signs with choreoathetoid movements and dystonia.

WOODHOUSE-SAKATI SYNDROME Is also known as hypogonadism, alopecia, diabetes mellitus, mental retardation, deafness, and extrapyramidal syndrome|extrapyramidal disorder, progressive, with primary hypogonadism, mental retardation, and alopecia|diabetes-hypogonadism-deafness-intellectual disability s

Related symptoms:

  • Intellectual disability
  • Seizures
  • Hearing impairment
  • Scoliosis
  • Hypertelorism


SOURCES: ORPHANET OMIM MESH MENDELIAN

More info about WOODHOUSE-SAKATI SYNDROME

Medium match GRANULOMATOSIS WITH POLYANGIITIS


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

Medium 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

Low match CONGENITAL FACTOR XII DEFICIENCY


Congenital factor XII deficiency is an autosomal recessive systemic dysfunction of the hemostatic pathway, that is due to a defect in the coagulation factor XII (FXII or Hageman factor), and is either asymptomatic or characterized by a prolonged activated partial thromboplastin time and an increased risk for thromboembolism. FXII deficiency is strongly associated with primary recurrent abortions.

CONGENITAL FACTOR XII DEFICIENCY Is also known as hageman factor deficiency|f12 deficiency|congenital hageman factor deficiency|haf deficiency

Related symptoms:

  • Pain
  • Edema
  • Headache
  • Abdominal pain
  • Abnormal bleeding


SOURCES: ORPHANET MESH OMIM MENDELIAN

More info about CONGENITAL FACTOR XII DEFICIENCY

Low match ALPORT SYNDROME, AUTOSOMAL DOMINANT


Alport syndrome classically comprises nephritis, often progressing to renal failure, and sensorineural hearing loss (Alport, 1927). For a general phenotypic description of Alport syndrome, see the X-linked dominant form (OMIM ). Approximately 85% of cases of Alport syndrome are X-linked and about 15% are autosomal recessive (OMIM ); autosomal dominant inheritance is rare (van der Loop et al., 2000).Also see benign familial hematuria (BFH ), a similar but milder disorder also caused by mutation in the COL4A3 gene.An autosomal dominant disorder sharing the clinical features of Alport syndrome but with the addition of macrothrombocytopenia, known as Fechtner syndrome (OMIM ), is caused by mutation in the MYH9 gene (OMIM ) on chromosome 22q11.

Related symptoms:

  • Hearing impairment
  • Sensorineural hearing impairment
  • Hypertension
  • Myopia
  • Renal insufficiency


SOURCES: OMIM MENDELIAN

More info about ALPORT SYNDROME, AUTOSOMAL DOMINANT

Low match HYPOBETALIPOPROTEINEMIA, FAMILIAL, 2; FHBL2


Hypobetalipoproteinemia (HBL) is defined as permanently low levels, below the 5th percentile of sex- and age-matched individuals in the population, of apolipoprotein B (apoB), total cholesterol, and low-density lipoprotein (LDL) cholesterol; the lipid profile in FHBL2 includes low HDL cholesterol as well. HBL can result from environmental factors such as a strict vegetarian diet, or can be secondary to certain diseases such as intestinal fat malabsorption, chronic pancreatitis, severe liver disease, malnutrition, or hyperthyroidism. Heritable primary causes of HBL include chylomicron retention disease (CMRD ), abetalipoproteinemia (OMIM ), and familial hypobetalipoproteinemia (FHBL) (summary by Martin-Campos et al., 2012).For a discussion of genetic heterogeneity of familial hypobetalipoproteinemia, see FHBL1 (OMIM ).

HYPOBETALIPOPROTEINEMIA, FAMILIAL, 2; FHBL2 Is also known as hypolipidemia, familial, combined

Related symptoms:

  • Respiratory tract infection
  • Abnormality of the liver
  • Malabsorption
  • Hepatic steatosis
  • Abnormality of the cardiovascular system


SOURCES: OMIM MESH MENDELIAN

More info about HYPOBETALIPOPROTEINEMIA, FAMILIAL, 2; FHBL2

Low match BUDD-CHIARI SYNDROME


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

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

Symptoms // Phenotype % cases
Pain Common - Between 50% and 80% cases
Seizures Uncommon - Between 30% and 50% cases
Headache Uncommon - Between 30% and 50% cases
Abdominal pain Uncommon - Between 30% and 50% cases
Pancreatitis Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases


Stroke Malabsorption Myalgia Vasculitis Renal insufficiency Fever Hypertension Diarrhea Splenomegaly Arthritis Weight loss Chest pain Cerebral ischemia Meningitis Purpura Gastrointestinal hemorrhage Intestinal obstruction Proteinuria Pericarditis Nausea and vomiting Arthralgia Sensorineural hearing impairment Hearing impairment Pleuritis Venous thrombosis Nephropathy

Rare Symptoms - Less than 30% cases


Gait disturbance Hyperreflexia Skin rash Thrombophlebitis Scarring Stage 5 chronic kidney disease Alopecia Erythema Fatigue Arterial thrombosis Sensory neuropathy Peripheral neuropathy Thromboembolism Nausea Ascites Peritonitis Nephrotic syndrome Orchitis Nephrocalcinosis Neoplasm Azotemia Rheumatoid arthritis Gastrointestinal infarctions Inflammation of the large intestine Elevated erythrocyte sedimentation rate Increased inflammatory response Acute hepatic failure Endocarditis Lymphadenopathy Vertigo Developmental regression Confusion Gangrene Pulmonary infiltrates Behavioral abnormality Glomerulonephritis Hemoptysis Mental deterioration Glomerulopathy Myositis Hemiplegia Systemic lupus erythematosus Hemiparesis Paralysis Memory impairment Migraine Cranial nerve paralysis Subcutaneous nodule Pleural effusion Dysarthria Cough Visual loss Hepatomegaly Retinopathy Arrhythmia Papule Paresthesia Visual impairment Hematuria Dyspnea Blindness Encephalitis Dilatation Glaucoma Acne Petechiae Reduced visual acuity Increased intracranial pressure Photophobia Mitral regurgitation Irritability Aortic regurgitation Joint stiffness Anorexia Abnormal pyramidal sign Abnormal blistering of the skin Recurrent corneal erosions Arteritis Cataract Rhinorrhea Abnormality of the nose Concave nasal ridge Blurred vision Angina pectoris Chronic obstructive pulmonary disease Nasal obstruction Inflammatory abnormality of the eye Elevated C-reactive protein level Tracheal stenosis Periorbital edema Ocular pain Ataxia Subglottic stenosis Granulomatosis Neuritis Ureteral stenosis Wheezing Abnormal oral cavity morphology Episcleritis Abnormality of the hypothalamus-pituitary axis Scleritis Recurrent intrapulmonary hemorrhage Prostatitis Epiphora Epididymitis Keratoconjunctivitis sicca Abnormality of the cardiovascular system Chronic pancreatitis Premature coronary artery atherosclerosis Decreased LDL cholesterol concentration Fat malabsorption Hyperthyroidism Malnutrition Hepatic steatosis Hypotriglyceridemia Abnormality of the liver Respiratory tract infection Diffuse glomerular basement membrane lamellation Lenticonus Thickening of the glomerular basement membrane Anterior polar cataract Abetalipoproteinemia Hypolipidemia Microscopic hematuria Varicose veins Reduced protein C activity Budd-Chiari syndrome Portal vein thrombosis Cholecystitis Esophageal varix Hypercoagulability Hepatocellular carcinoma Acute respiratory tract infection Polycythemia Portal hypertension Cirrhosis Carcinoma Elevated hepatic transaminase Jaundice Macrothrombocytopenia Hypophosphatemia Pulmonary embolism Alopecia areata Anterior uveitis Optic neuritis Chorioretinitis Immunologic hypersensitivity Erythema nodosum Oral ulcer Stomatitis Iridocyclitis Recurrent aphthous stomatitis Abnormal myocardium morphology Raynaud phenomenon Pustule Uveitis Aseptic necrosis Posterior uveitis Iritis Nephritis Deep venous thrombosis Myopia Prolonged whole-blood clotting time Retinal vein occlusion Reduced factor XII activity Prolonged partial thromboplastin time Allergy Abnormal bleeding Retrobulbar optic neuritis Edema Hypopyon Decreased level of D-mannose in urine Pulmonary fibrosis Genital ulcers Panuveitis Superficial thrombophlebitis Restrictive ventilatory defect Decreased serum estradiol Diabetes insipidus Congenital hypoplastic anemia Leukocytosis Hyperkalemia Amyloidosis Episodic fever Increased serum ferritin Gout Antinuclear antibody positivity Edema of the lower limbs Oral leukoplakia Anemia of inadequate production Decreased circulating aldosterone level Synovitis Stiff neck Erysipelas Osteoarthritis Renal amyloidosis Serositis Recurrent meningitis Intellectual disability Scoliosis Hypertelorism Cognitive impairment High palate Delayed speech and language development Downslanted palpebral fissures Frontal bossing Dystonia Intellectual disability, mild Chronic kidney disease Asthma Babinski sign Transient ischemic attack Motor delay Tremor Dementia Facial palsy Chorea Intracranial hemorrhage Personality changes Heart murmur Cutis marmorata Aphasia Visual field defect Atrophic scars Thrombocytosis Acrocyanosis Abnormality of the kidney Arteriovenous malformation Peripheral arterial stenosis Facial paralysis Hemianopia Arterial stenosis Thromboembolic stroke Amaurosis fugax Vascular skin abnormality Antiphospholipid antibody positivity Lupus anticoagulant Anemia Constipation Acidosis Hepatosplenomegaly Abnormality of metabolism/homeostasis Hypogonadism Stridor Hypoplasia of the fallopian tube Hypoplasia of the uterus Autoimmune thrombocytopenia Insulin-resistant diabetes mellitus Heart block Anodontia Decreased serum testosterone level Muscle weakness Abnormal T-wave Abnormal spermatogenesis Increased thyroid-stimulating hormone level Streak ovary Decreased serum insulin-like growth factor 1 Progressive extrapyramidal movement disorder Progressive alopecia Flat occiput Respiratory insufficiency Respiratory distress Cardiomyopathy Recurrent respiratory infections Proptosis Hydronephrosis Otitis media Epistaxis Diplopia Sinusitis Skin ulcer Hoarse voice Conjunctivitis Chronic otitis media Aplasia/Hypoplasia of the eyebrow Sparse eyebrow Diabetes mellitus Prominent nose Micropenis Hypothyroidism High forehead Camptodactyly Protruding ear Sparse hair Prominent nasal bridge Arthrogryposis multiplex congenita Hypotrichosis Delayed puberty Abnormality of movement Polyneuropathy Triangular face Dental malocclusion Premature ovarian insufficiency Decreased testicular size Amenorrhea Dehydration Bilateral sensorineural hearing impairment Abnormality of extrapyramidal motor function Psychosis Fine hair Primary amenorrhea Sparse scalp hair Choreoathetosis Hallucinations Hypergonadotropic hypogonadism Hypogonadotrophic hypogonadism Hyperlipidemia Hepatic vein thrombosis



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