Hypertension, and Myocardial infarction

Diseases related with Hypertension and Myocardial infarction

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

Top matches:

Coronary artery disease (CAD) and its most important complication, acute myocardial infarction (MI), are leading causes of death and disability in the developed world. Multiple risk factors for CAD/MI have been identified, including family history, hypertension, hypercholesterolemia, obesity, smoking, and diabetes. Several genomewide scans of affected sib pairs have identified susceptibility loci for CAD, e.g., {607339} and {300464}.

CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1; ADCAD1 Is also known as coronary artery disease with myocardial infarction

Related symptoms:

  • Hypertension
  • Obesity
  • Chest pain
  • Myocardial infarction
  • Hypercholesterolemia


SOURCES: OMIM MESH MENDELIAN

More info about CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1; ADCAD1

ABDOMINAL OBESITY-METABOLIC SYNDROME 3; AOMS3 Is also known as central obesity, type 2 diabetes, hypertension, and early-onset coronary artery disease

Related symptoms:

  • Hypertension
  • Obesity
  • Stroke
  • Type II diabetes mellitus
  • Myocardial infarction


SOURCES: OMIM MENDELIAN

More info about ABDOMINAL OBESITY-METABOLIC SYNDROME 3; AOMS3

A degenerative disease of the brain characterized by the insidious onset of dementia. Impairment of memory, judgment, attention span, and problem solving skills are followed by severe apraxia and a global loss of cognitive abilities. The condition primarily occurs after age 60, and is marked pathologically by severe cortical atrophy and the triad of senile plaques, neurofibrillary tangles, and neuropil threads. [HPO:probinson]

ALZHEIMER DISEASE 2; AD2 Is also known as alzheimer disease associated with apoe4|alzheimer disease 2, late-onset

Related symptoms:

  • Hypertension
  • Dementia
  • Diabetes mellitus
  • Stroke
  • Parkinsonism


SOURCES: OMIM MESH MENDELIAN

More info about ALZHEIMER DISEASE 2; AD2

Other less relevant matches:

Liddle syndrome is an autosomal dominant disorder characterized by early-onset salt-sensitive hypertension, hypokalemia, metabolic alkalosis, and suppression of plasma renin activity and aldosterone secretion (summary by Yang et al., 2014). Genetic Heterogeneity of Liddle SyndromeLiddle syndrome-2 (OMIM ) is caused by mutation in the SCNN1G gene (OMIM ), which encodes the ENaC gamma subunit. Liddle syndrome-3 (OMIM ) is caused by mutation in the SCNN1A gene (OMIM ), which encodes the ENaC alpha subunit.Hanukoglu and Hanukoglu (2016) provided a detailed review of the ENaC gene family, including structure, function, tissue distribution, and associated inherited diseases.

LIDDLE SYNDROME 1; LIDLS1 Is also known as lidls|liddle syndrome|pseudoaldosteronism|pseudohyperaldosteronism

Related symptoms:

  • Hypertension
  • Renal insufficiency
  • Stroke
  • Stage 5 chronic kidney disease
  • Abnormality of the cardiovascular system


SOURCES: OMIM MENDELIAN

More info about LIDDLE SYNDROME 1; LIDLS1

AORTIC ANEURYSM, FAMILIAL THORACIC 6; AAT6 Is also known as familial thoracic aortic aneurysm with livedo reticularis and iris flocculi

Related symptoms:

  • Hypertension
  • Dilatation
  • Patent ductus arteriosus
  • Coloboma
  • Myocardial infarction


SOURCES: OMIM MESH MENDELIAN

More info about AORTIC ANEURYSM, FAMILIAL THORACIC 6; AAT6

Related symptoms:

  • Hypertension
  • Osteoporosis
  • Diabetes mellitus
  • Stroke
  • Sudden cardiac death


SOURCES: OMIM MESH MENDELIAN

More info about CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT 2; ADCAD2

Related symptoms:

  • Intellectual disability
  • Hypertension
  • Congestive heart failure
  • Obesity
  • Diabetes mellitus


SOURCES: OMIM ORPHANET MENDELIAN

More info about OBESITY DUE TO CEP19 DEFICIENCY

Paget disease of bone-6 is an autosomal dominant disorder characterized by adult onset of bone pain associated with polyostotic bone lesions primarily affecting the axial skeleton. A subset of patients can develop coronary artery disease and/or malignant giant cell tumor (GCT) of the bone, which arises within the Paget bone lesions (summary by Divisato et al., 2016).For a general phenotypic description and a discussion of genetic heterogeneity of Paget disease of bone, see {167250}.

Related symptoms:

  • Hearing impairment
  • Neoplasm
  • Pain
  • Hypertension
  • Recurrent fractures


SOURCES: OMIM MENDELIAN

More info about PAGET DISEASE OF BONE 6; PDB6

Abdominal aortic aneurysm is a multifactorial disorder with multiple genetic and environmental risk factors. The disorder may occur as part of a heritable syndrome or in isolation (summary by Kuivaniemi et al., 2003). Genetic Heterogeneity of Abdominal Aortic AneurysmMapped loci for abdominal aortic aneurysm include AAA1 on chromosome 19q13; AAA2 (OMIM ) on chromosome 4q31; AAA3 (OMIM ) on chromosome 9p21; and AAA4 (OMIM ) on chromosome 12q13.

FAMILIAL ABDOMINAL AORTIC ANEURYSM Is also known as aneurysm, abdominal aortic|aaa|abdominal aortic aneurysm

Related symptoms:

  • Pain
  • Cataract
  • Hypertension
  • Vomiting
  • Dilatation


SOURCES: ORPHANET OMIM MENDELIAN

More info about FAMILIAL ABDOMINAL AORTIC ANEURYSM

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

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

Symptoms // Phenotype % cases
Stroke Uncommon - Between 30% and 50% cases
Diabetes mellitus Uncommon - Between 30% and 50% cases
Hypercholesterolemia Uncommon - Between 30% and 50% cases
Obesity Uncommon - Between 30% and 50% cases
Type II diabetes mellitus Uncommon - Between 30% and 50% cases

Other less frequent symptoms

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

Rare Symptoms - Less than 30% cases

Pain Hearing impairment Renal insufficiency Hypertriglyceridemia Nephrocalcinosis Premature coronary artery atherosclerosis Thoracic aortic aneurysm Aortic aneurysm Dilatation Abnormality of the cardiovascular system Stage 5 chronic kidney disease Atherosclerosis Agnosia Nephrolithiasis Vomiting Cataract Coronary artery atherosclerosis Elevated alkaline phosphatase Chest pain Bone pain Left ventricular hypertrophy Nausea Osteoarthritis Recurrent fractures Truncal obesity Neoplasm Abdominal obesity Increased LDL cholesterol concentration Decreased HDL cholesterol concentration Hernia Tachycardia Azoospermia Nephritis Lenticonus Azotemia Thickening of the glomerular basement membrane Anterior polar cataract Macrothrombocytopenia Microscopic hematuria Hypophosphatemia Glomerulonephritis Shock Nephrotic syndrome Hematuria Proteinuria Myopia Sensorineural hearing impairment Abdominal aortic aneurysm Peripheral arterial stenosis Oligospermia Insulin resistance Long-tract signs Hypokalemic alkalosis Bicuspid aortic valve Coloboma Patent ductus arteriosus Alzheimer disease Nephrosclerosis Hypokalemic metabolic alkalosis Pseudohypoaldosteronism Cutis marmorata Decreased circulating renin level Decreased circulating aldosterone level Metabolic alkalosis Alkalosis Hyperaldosteronism Hypokalemia Neurofibrillary tangles Apraxia Aortic dissection Hepatic steatosis Coronary artery stenosis Infertility Abnormality of the liver Congestive heart failure Intellectual disability Gout Glucose intolerance Hyperlipidemia Dementia Ascending tubular aorta aneurysm Sudden cardiac death Osteoporosis Iris flocculi Moyamoya phenomenon Ascending aortic dissection Parkinsonism Memory impairment Diffuse glomerular basement membrane lamellation


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