Fever, and Aortic valve stenosis

Diseases related with Fever and Aortic valve stenosis

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

Top matches:

Familial bicuspid aortic valve is a rare, genetic, aortic malformation defined as a presence of abnormal two-leaflet aortic valve in at least 2 first-degree relatives. It is frequently asymptomatic or may be associated with progressive aortic valve disease (aortic regurgitation and/or aortic stenosis, typically due to valve calcification) and a concomitant aortopathy (i.e. aortic dilation, aortic aneurysm and/or dissection).

FAMILIAL BICUSPID AORTIC VALVE Is also known as aortic valve, calcification of|aortic stenosis, calcific|aortic valve, bicuspid|familial bav|bav|bicuspid aortic valve|aortic valve disease

Related symptoms:

  • Hypertension
  • Fever
  • Ventricular septal defect
  • Cardiomyopathy
  • Atrial septal defect


SOURCES: ORPHANET OMIM MENDELIAN

More info about FAMILIAL BICUSPID AORTIC VALVE

Prader-Willi syndrome is characterized by diminished fetal activity, obesity, muscular hypotonia, mental retardation, short stature, hypogonadotropic hypogonadism, and small hands and feet. It can be considered to be an autosomal dominant disorder and is caused by deletion or disruption of a gene or several genes on the proximal long arm of the paternal chromosome 15 or maternal uniparental disomy 15, because the gene(s) on the maternal chromosome(s) 15 are virtually inactive through imprinting. Horsthemke and Wagstaff (2008) provided a detailed review of the mechanisms of imprinting of the Prader-Willi/Angelman syndrome (OMIM ) region.See also the chromosome 15q11-q13 duplication syndrome (OMIM ), which shows overlapping clinical features.

PRADER-WILLI SYNDROME; PWS Is also known as prader-labhart-willi syndrome

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Generalized hypotonia


SOURCES: OMIM MENDELIAN

More info about PRADER-WILLI SYNDROME; PWS

Hypermethioninemia due to methionine adenosyltransferase deficiency is a very rare metabolic disorder resulting in isolated hepatic hypermethioninemia that is usually benign due to partial inactivation of enzyme activity. Rarely patients have been found to have an odd odor or neurological disorders such as brain demyelination.

BRAIN DEMYELINATION DUE TO METHIONINE ADENOSYLTRANSFERASE DEFICIENCY Is also known as mat deficiency|mat i/iii deficiency|hypermethioninemia, isolated persistent|methionine adenosyltransferase deficiency

Related symptoms:

  • Intellectual disability
  • Growth delay
  • Nystagmus
  • Cognitive impairment
  • Hyperreflexia


SOURCES: OMIM ORPHANET MENDELIAN

More info about BRAIN DEMYELINATION DUE TO METHIONINE ADENOSYLTRANSFERASE DEFICIENCY

Other less relevant matches:

Medium match TAKAYASU ARTERITIS

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

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

Medium match FABRY DISEASE

Fabry disease (FD) is a progressive, inherited, multisystemic lysosomal storage disease characterized by specific neurological, cutaneous, renal, cardiovascular, cochleo-vestibular and cerebrovascular manifestations.

FABRY DISEASE Is also known as ceramide trihexosidase deficiency|hereditary dystopic lipidosis|fd|alpha-galactosidase a deficiency|diffuse angiokeratoma|gla deficiency|angiokeratoma corporis diffusum|anderson-fabry disease

Related symptoms:

  • Seizures
  • Short stature
  • Hearing impairment
  • Sensorineural hearing impairment
  • Pain


SOURCES: ORPHANET OMIM MESH MENDELIAN

More info about FABRY DISEASE

Idiopathic pulmonary fibrosis (IPF) is a nonneoplastic pulmonary disease that is characterized by the formation of scar tissue within the lungs in the absence of any known cause.

IDIOPATHIC PULMONARY FIBROSIS Is also known as cfa|uip|usual interstitial pneumonia|interstitial pneumonitis, usual|idiopathic pulmonary fibrosis, familial|cryptogenic fibrosing alveolitis|fibrosing alveolitis, cryptogenic|fibrocystic pulmonary dysplasia

Related symptoms:

  • Neoplasm
  • Hypertension
  • Fever
  • Respiratory insufficiency
  • Respiratory distress


SOURCES: OMIM ORPHANET MENDELIAN

More info about IDIOPATHIC PULMONARY FIBROSIS

Cataract-glaucoma syndrome is characterised by the association of total bilateral congenital cataract with the secondary occurrence of glaucoma appearing at ages varying between 10 and 40 years.

Related symptoms:

  • Seizures
  • Short stature
  • Generalized hypotonia
  • Pain
  • Feeding difficulties


SOURCES: ORPHANET MENDELIAN

More info about CATARACT-GLAUCOMA SYNDROME

Familial atrial myxoma is a rare, genetic cardiac tumor characterized by the presence of a primary, benign, gelatinous mass located in the atria and composed of primitive connective tissue cells and stroma (resembling mesenchyme) in several members of a family. Clinical presentation depends on the size, mobility and location of tumor, ranging from nonspecific and/or constitutional symptoms to sudden cardiac death, and includes dyspnea, hemoptisis, syncope, fatigue, fever, cutaneous rash, increases in venous pressure and/or peripheral edema.

FAMILIAL ATRIAL MYXOMA Is also known as atrial myxoma, familial

Related symptoms:

  • Seizures
  • Cognitive impairment
  • Fever
  • Atrial septal defect
  • Congestive heart failure


SOURCES: MESH OMIM ORPHANET MENDELIAN

More info about FAMILIAL ATRIAL MYXOMA

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

Top 5 symptoms//phenotypes associated to Fever and Aortic valve stenosis

Symptoms // Phenotype % cases
Dilatation Common - Between 50% and 80% cases
Hypertension Common - Between 50% and 80% cases
Headache Common - Between 50% and 80% cases
Seizures Common - Between 50% and 80% cases
Congestive heart failure Uncommon - Between 30% and 50% cases

Other less frequent symptoms

Patients with Fever and Aortic valve stenosis. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases

Aortic regurgitation Arthralgia Arthritis Chest pain Behavioral abnormality Anorexia Myocardial infarction Fatigue Cognitive impairment Pain Abnormal heart valve morphology Vasculitis Neoplasm Abnormal myocardium morphology Subcutaneous nodule Weight loss Respiratory failure Vomiting Increased inflammatory response Diarrhea Abdominal pain Nausea and vomiting Edema Cough Mitral regurgitation Short stature Dyspnea Hypertrophic cardiomyopathy Abnormality of the nervous system Migraine Respiratory tract infection Ischemic stroke Heart murmur Stroke Myalgia Interstitial pulmonary abnormality

Rare Symptoms - Less than 30% cases

Hepatitis Hyperreflexia Abnormality of lipid metabolism Pulmonary embolism Renal insufficiency Inflammation of the large intestine Spontaneous abortion Bradycardia Cataract Developmental regression Arteritis Abnormal endocardium morphology Anemia Pulmonary arterial hypertension Inflammatory abnormality of the eye Abnormal aortic valve morphology Hyperhidrosis Cerebral ischemia Retinopathy Gangrene Hemoptysis Ascending tubular aorta aneurysm Malabsorption Irritability Tubulointerstitial nephritis Abnormal lung morphology Easy fatigability Clubbing Tricuspid regurgitation Coronary artery atherosclerosis Elevated erythrocyte sedimentation rate Aortic root aneurysm Edema of the lower limbs Clubbing of fingers Syncope Chronic pain Respiratory distress Pneumonia Scaling skin Exertional dyspnea Pulmonary insufficiency Jaundice Cholestasis Mitral valve prolapse Hematuria Erythema Cranial nerve paralysis Scarring Papule Gastrointestinal hemorrhage Paresthesia Confusion Lymphadenopathy Vertigo Meningitis Increased intracranial pressure Skin rash Glomerulopathy Pulmonary infiltrates Endocarditis Sensorineural hearing impairment Respiratory insufficiency Arrhythmia Constipation Carcinoma Proteinuria Abnormality of the cardiovascular system Pericarditis Atrial septal defect Photophobia Delayed puberty Nystagmus Pruritus Growth delay Cardiomyopathy Generalized hypotonia Bicuspid aortic valve Feeding difficulties Intellectual disability Asymmetric septal hypertrophy Abnormality of the dentition Oligospermia Angina pectoris Hypoplastic left heart Peripheral arterial stenosis Reduced ejection fraction Heat intolerance Supraventricular tachycardia Wheezing Large earlobe Renal tubular dysfunction Double outlet right ventricle Aortic dissection Abnormality of the gastrointestinal tract Abnormal EKG Xerostomia Tubular atrophy Chronic obstructive pulmonary disease Transient ischemic attack Elevated serum creatinine Mitral stenosis Sepsis Achalasia Aortic aneurysm Abnormality of cardiovascular system physiology Biventricular hypertrophy Primary hypothyroidism Microalbuminuria Conjunctival telangiectasia Supraventricular arrhythmia Dysesthesia Abnormal cornea morphology Abnormality of the renal tubule Abnormal thrombosis Tubulointerstitial fibrosis Abnormal renal physiology Sinus bradycardia Miosis T-wave inversion Gastrointestinal dysmotility Periorbital fullness Abnormal mitral valve morphology High-frequency hearing impairment Restrictive cardiomyopathy Abnormality of the nose Abnormality of femur morphology Renal tubular acidosis Myocardial fibrosis Chronic fatigue Orthostatic hypotension Glycosuria Left ventricular hypertrophy Progressive hearing impairment Abnormal intestine morphology Ventricular tachycardia Hyperlipidemia Purpura Aminoaciduria Exercise intolerance Abnormal autonomic nervous system physiology Fasciculations Lymphedema Hypohidrosis Mitral atresia Cystic medial necrosis Palpitations Atrial fibrillation Thick lower lip vermilion Ventricular hypertrophy Nephrotic syndrome Abnormality of the left ventricular outflow tract Hypotension Urinary incontinence Bicuspid pulmonary valve Sudden cardiac death Abdominal distention Muscle cramps Corneal dystrophy Reduced bone mineral density Telangiectasia of the skin Diabetes insipidus Celiac disease Vascular skin abnormality Progressive sensorineural hearing impairment Thoracic aortic aneurysm Aortic valve calcification Impotence Bundle branch block Loss of consciousness Emphysema Anhidrosis Polyuria Aortic arch aneurysm Ventricular arrhythmia Impaired vibratory sensation Ascending aortic dissection Personality changes Polydipsia Glomerulosclerosis Hemiplegia Abnormality of the hand Prominent supraorbital ridges Chronic kidney disease Atrioventricular block Hypoplastic aortic arch Tinnitus Decreased female libido Abnormality of temperature regulation Retinal vascular tortuosity Cardiomegaly Cardiac myxoma Bacterial endocarditis Orthopnea Pulmonary edema Subarachnoid hemorrhage Growth hormone excess Dilatation of the cerebral artery Thromboembolism Cerebral hemorrhage Neoplasm of the skin Ventricular septal defect Ascites Ptosis Coma Abnormality of skin pigmentation Premature loss of primary teeth Chondrocalcinosis Papilledema Premature loss of teeth Osteomalacia Rickets Hypercalcemia Bone pain Waddling gait Pulmonic valve myxoma Decreased liver function Proptosis Abnormal pericardium morphology Aseptic leukocyturia Strawberry tongue Double outlet right ventricle with subpulmonary ventricular septal defect without pulmonary stenosis Abnormal emotion/affect behavior Pyuria Arthralgia/arthritis Abnormality of nail color Coronary artery aneurysm Cervical lymphadenopathy CSF pleocytosis Conjunctival hyperemia Glossitis Conjunctivitis Abnormal oral mucosa morphology Cholecystitis Synovitis Cheilitis Elevated C-reactive protein level Recurrent pharyngitis Allergy Myocarditis Acute kidney injury Leukocytosis Hyponatremia Hypoalbuminemia Craniosynostosis Brachycephaly Corneal crystals Shortened QT interval Abnormality of glycosphingolipid metabolism Impaired renal concentrating ability Functional abnormality of the gastrointestinal tract ST segment depression Unexplained fevers Mucosal telangiectasiae Concentric hypertrophic cardiomyopathy Coronary artery stenosis Shortened PR interval Decreased lacrimation Angiokeratoma corporis diffusum Hyposthenuria Hyperkeratotic papule Impaired temperature sensation Obstructive lung disease Angiokeratoma Reduced sperm motility Increased blood urea nitrogen Distal renal tubular acidosis Vascular tortuosity Decreased glomerular filtration rate Nephrogenic diabetes insipidus Thoracic aorta calcification Limb pain Abnormality of the forehead Tortuosity of conjunctival vessels Ground-glass opacification on pulmonary HRCT Bronchiectasis Honeycomb lung Reticular pattern on pulmonary HRCT Hypocapnia Alveolar cell carcinoma Crackles Right ventricular failure Polycythemia Abnormal heart morphology Increased antibody level in blood Pulmonary fibrosis Coarctation of aorta Cyanosis Left ventricular septal hypertrophy Cirrhosis Gastroesophageal reflux Cornea verticillata Abnormal glomerular filtration rate Abnormality of the common coagulation pathway Increased glomerular filtration rate Increased carotid artery intimal medial thickness Abnormal ST segment Abnormal common carotid artery morphology Acroparesthesia Heavy proteinuria Tenesmus Nephropathy Nausea Thick vermilion border Temperature instability Dystonia Tremor Polymicrogyria Acromicria Poor gross motor coordination Almond-shaped palpebral fissure Hypopnea Narrow palm Psychotic episodes Hypoplastic labia minora Central adrenal insufficiency Triangular mouth Abnormality of the eye Disseminated intravascular coagulation Erysipelas Frontal upsweep of hair Clitoral hypoplasia Anteverted ears Poor fine motor coordination Abdominal obesity Cor pulmonale Generalized hypopigmentation Hypothermia Ocular albinism Arachnodactyly Abnormality of the liver Hypoplasia of the fovea Hypermetropia Psoriasiform dermatitis Thin upper lip vermilion Skin ulcer Hypoglycemia Neonatal hypotonia Apnea Abnormality of the pinna Neurological speech impairment Attention deficit hyperactivity disorder Leukemia Dolichocephaly Carious teeth Abnormality of eye movement Muscle weakness Halitosis Hypermethioninemia Hypertyrosinemia Homocystinuria CNS demyelination Gout Dysdiadochokinesis Genu valgum Infertility Peripheral demyelination Chromosome breakage Acrocyanosis Narrow mouth Psychosis Scrotal hypoplasia Sleep apnea Narrow palpebral fissure Short foot Hypogonadotrophic hypogonadism Increased body weight Tapered finger Insulin resistance Clumsiness Primary amenorrhea Cutaneous photosensitivity Type II diabetes mellitus Poor suck Decreased fetal movement Oligohydramnios Narrow forehead Sleep disturbance Amenorrhea Specific learning disability Hip dysplasia Febrile seizures Growth hormone deficiency Esotropia Hypopigmentation of the skin Infantile muscular hypotonia Nasal speech Oligomenorrhea Polyphagia Overweight Central hypotonia Short palm Iris hypopigmentation Hypoventilation Hypopigmentation of hair Downturned corners of mouth Striae distensae Impaired pain sensation Myeloid leukemia Narrow nasal bridge External genital hypoplasia Failure to thrive in infancy Truncal obesity Decreased muscle mass Adrenal insufficiency Skeletal muscle hypertrophy Albinism Glucose intolerance Small hand Large hands Emotional lability Radial deviation of finger Hyperinsulinemia Precocious puberty Osteopenia Autism Thick eyebrow Pleuritis Orchitis Retrobulbar optic neuritis Iritis Iridocyclitis Posterior uveitis Anterior uveitis Optic neuritis Chorioretinitis Immunologic hypersensitivity Erythema nodosum Thrombophlebitis Oral ulcer Panuveitis Micrognathia Alopecia areata Stomatitis Recurrent aphthous stomatitis Arterial thrombosis Strabismus Myositis Raynaud phenomenon Abnormal facial shape Pustule Uveitis Superficial thrombophlebitis Genital ulcers Muscular hypotonia Mandibular prognathia Bulbous nose Tachycardia Full cheeks Stage 5 chronic kidney disease Abnormality of the cerebral white matter Corneal opacity Prominent nasal bridge Abnormality of the kidney Global developmental delay Anxiety Coarse facial features Hypothyroidism Epididymitis Hyperkeratosis Posteriorly rotated ears Scoliosis Depressivity Midface retrusion Optic atrophy Peripheral neuropathy Failure to thrive Hearing impairment Hypopyon Decreased level of D-mannose in urine Aseptic necrosis Keratoconjunctivitis sicca Micropenis Ataxia Reduced visual acuity Glaucoma Obesity Alopecia Visual loss Clinodactyly Splenomegaly Hyporeflexia Blindness Gait disturbance Recurrent respiratory infections Prominent forehead Short nose Hypertensive crisis Osteoporosis Gastrointestinal infarctions Amaurosis fugax Upslanted palpebral fissure Hypogonadism Arterial stenosis Abnormal pattern of respiration Diabetes mellitus Hyperactivity Reduced consciousness/confusion Syndactyly Kyphosis Cryptorchidism Hemiparesis Blurred vision Epiphora Acne Rheumatoid arthritis Pleural effusion Encephalitis High palate Venous thrombosis Pancreatitis Delayed speech and language development Motor delay Abnormal blistering of the skin Intellectual disability, mild Memory impairment Depressed nasal bridge Epicanthus Myopia Intrauterine growth retardation Talipes equinovarus Ventriculomegaly Intellectual disability, severe Myopathy Abnormal pyramidal sign Autoimmunity Joint stiffness Abnormal gallbladder morphology


If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like Microphthalmia and Microdontia, related diseases and genetic alterations Fever and Syncope, related diseases and genetic alterations