Congestive heart failure, and Eosinophilia

Diseases related with Congestive heart failure and Eosinophilia

In the following list you will find some of the most common rare diseases related to Congestive heart failure and Eosinophilia that can help you solving undiagnosed cases.


Top matches:

Medium match CONGENITAL CATARACT-HYPERTROPHIC CARDIOMYOPATHY-MITOCHONDRIAL MYOPATHY SYNDROME


Congenital cataract - hypertrophic cardiomyopathy - mitochrondrial myopathy (CCM) is a mitochondrial disease (see this term) characterized by cataracts, hypertrophic cardiomyopathy, muscle weakness and lactic acidosis after exercise.

CONGENITAL CATARACT-HYPERTROPHIC CARDIOMYOPATHY-MITOCHONDRIAL MYOPATHY SYNDROME Is also known as mtdps10|sengers syndrome|cardiomyopathy and cataract|mitochondrial dna depletion syndrome 10 (cardiomyopathic type)

Related symptoms:

  • Intellectual disability
  • Seizures
  • Generalized hypotonia
  • Growth delay
  • Nystagmus


SOURCES: OMIM ORPHANET MENDELIAN

More info about CONGENITAL CATARACT-HYPERTROPHIC CARDIOMYOPATHY-MITOCHONDRIAL MYOPATHY SYNDROME

Medium match INCONTINENTIA PIGMENTI


Incontinentia pigmenti (IP) is a rare X-linked dominant multi-systemic ectodermal dysplasia usually lethal in males and presenting neonatally in females with a bullous rash along Blashko's lines (BL) followed by verrucous plaques evolving over time to hyperpigmented swirling patterns. It is further characterized by teeth abnormalities, alopecia, nail dystrophy and affects occasionally the retina and the central nervous system (CNS).

INCONTINENTIA PIGMENTI Is also known as bloch-siemens syndrome|bloch-sulzberger syndrome

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Scoliosis


SOURCES: ORPHANET MENDELIAN

More info about INCONTINENTIA PIGMENTI

Medium match SARCOIDOSIS


Sarcoidosis is a multisystemic disorder of unknown cause characterized by the formation of immune granulomas in involved organs.

SARCOIDOSIS Is also known as boeck sarcoid|besnier-boeck-schaumann disease|sarcoidosis|boeck's sarcoid

Related symptoms:

  • Seizures
  • Pain
  • Cataract
  • Anemia
  • Visual impairment


SOURCES: ORPHANET OMIM MENDELIAN

More info about SARCOIDOSIS

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Other less relevant matches:

Medium match POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY; PGBM1


Polyglucosan body myopathy-1 is an autosomal recessive disorder characterized by onset in childhood of progressive proximal muscle weakness, resulting in difficulties in ambulation. Most patients also develop progressive dilated cardiomyopathy, which may necessitate cardiac transplant in severe cases. A small subset of patients present with severe immunodeficiency and a hyperinflammatory state in very early childhood (summary by Boisson et al., 2012 and Nilsson et al., 2013). Genetic Heterogeneity of Polyglucosan Body MyopathySee also PGBM2 (OMIM ), caused by mutation in the GYG1 gene (OMIM ) on chromosome 3q24.

POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY; PGBM1 Is also known as polyglucosan body myopathy, early-onset, with or without immunodeficiency|pbmei

Related symptoms:

  • Scoliosis
  • Growth delay
  • Failure to thrive
  • Muscle weakness
  • Ptosis


SOURCES: OMIM MENDELIAN

More info about POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY; PGBM1

Medium match PRIMARY SCLEROSING CHOLANGITIS


Primary sclerosing cholangitis (PSC) is a rare, slowly progressive liver disease characterized by inflammation and destruction of the intra- and/or extra-hepatic bile ducts that lead to cholestasis, liver fibrosis, liver cirrhosis and ultimately liver failure.

PRIMARY SCLEROSING CHOLANGITIS Is also known as psc

Related symptoms:

  • Pain
  • Hypertension
  • Hepatomegaly
  • Fever
  • Fatigue


SOURCES: ORPHANET OMIM MENDELIAN

More info about PRIMARY SCLEROSING CHOLANGITIS

Medium match WHIM SYNDROME


WHIM (warts, hypogammaglobulinemia, infections, and myelokathexis) syndrome is a congenital autosomal dominant immune deficiency characterized by abnormal retention of mature neutrophils in the bone marrow (myelokathexis) and occasional hypogammaglobulinemia, associated with an increased risk for bacterial infections and a susceptibility to human papillomavirus (HPV) induced lesions (cutaneous warts, genital dysplasia and invasive mucosal carcinoma).

WHIM SYNDROME Is also known as warts, hypogammaglobulinemia, infections, and myelokathexis syndrome|warts-infections-leukopenia-myelokatexis syndrome|wilm|warts-hypogammaglobulinemia-infections-myelokathexis syndrome

Related symptoms:

  • Hearing impairment
  • Neoplasm
  • Fever
  • Congestive heart failure
  • Immunodeficiency


SOURCES: MESH OMIM ORPHANET MENDELIAN

More info about WHIM SYNDROME

Medium 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

Low match GAUCHER DISEASE TYPE 1


Gaucher disease type 1 is the chronic non-neurological form of Gaucher disease (GD; see this term) characterized by organomegaly, bone involvement and cytopenia.

GAUCHER DISEASE TYPE 1 Is also known as gaucher disease, juvenile and adult, cerebral|gd iii|gaucher disease, chronic neuronopathic type|non-cerebral juvenile gaucher disease|gaucher disease, subacute neuronopathic type

Related symptoms:

  • Seizures
  • Global developmental delay
  • Short stature
  • Scoliosis
  • Ataxia


SOURCES: ORPHANET OMIM MENDELIAN

More info about GAUCHER DISEASE TYPE 1

Low match NOONAN SYNDROME 1; NS1


Noonan syndrome (NS) is an autosomal dominant disorder characterized by short stature, facial dysmorphism, and a wide spectrum of congenital heart defects. The distinctive facial features consist of a broad forehead, hypertelorism, downslanting palpebral fissures, a high-arched palate, and low-set, posteriorly rotated ears. Cardiac involvement is present in up to 90% of patients. Pulmonic stenosis and hypertrophic cardiomyopathy are the most common forms of cardiac disease, but a variety of other lesions are also observed. Additional relatively frequent features include multiple skeletal defects (chest and spine deformities), webbed neck, mental retardation, cryptorchidism, and bleeding diathesis (summary by Tartaglia et al., 2002). Genetic Heterogeneity of Noonan SyndromeSee also NS3 (OMIM ), caused by mutation in the KRAS gene (OMIM ); NS4 (OMIM ), caused by mutation in the SOS1 gene (OMIM ); NS5 (OMIM ), caused by mutation in the RAF1 gene (OMIM ); NS6 (OMIM ), caused by mutation in the NRAS gene (OMIM ); NS7 (OMIM ), caused by mutation in the BRAF gene (OMIM ); NS8 (OMIM ), caused by mutation in the RIT1 gene (OMIM ); NS9 (OMIM ), caused by mutation in the SOS2 gene (OMIM ); and NS10 (OMIM ), caused by mutation in the LZTR1 gene (OMIM ).See also NS2 (OMIM ) for a possible autosomal recessive form of NS; Noonan syndrome-like disorder with loose anagen hair-1 (NSLH1 ), caused by mutation in the SHOC2 gene (OMIM ); Noonan syndrome-like disorder with loose anagen hair-2 (NSLH2 ), caused by mutation in the PPP1CB gene (OMIM ); and Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia (NSLL ), caused by mutation in the CBL gene (OMIM ).Mutations in the neurofibromin gene (NF1 ), which is the site of mutations causing classic neurofibromatosis type I (NF1 ), have been found in neurofibromatosis-Noonan syndrome (NFNS ).

NOONAN SYNDROME 1; NS1 Is also known as female pseudo-turner syndrome|male turner syndrome|noonan syndrome|turner phenotype with normal karyotype

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Microcephaly


SOURCES: OMIM MENDELIAN

More info about NOONAN SYNDROME 1; NS1

Low match FAMILIAL ISOLATED DILATED CARDIOMYOPATHY


Familial isolated dilated cardiomyopathy is a rare, genetically heterogeneous cardiac disease characterized by dilatation leading to systolic and diastolic dysfunction of the left and/or right ventricles, causing heart failure or arrhythmia.

FAMILIAL ISOLATED DILATED CARDIOMYOPATHY Is also known as cardiomyopathy, familial dilated|cardiomyopathy, familial dilated, 1|cmpd1|familial or idiopathic dilated cardiomyopathy|fdc

Related symptoms:

  • Sensorineural hearing impairment
  • Feeding difficulties
  • Fatigue
  • Ventriculomegaly
  • Cardiomyopathy


SOURCES: OMIM ORPHANET MENDELIAN

More info about FAMILIAL ISOLATED DILATED CARDIOMYOPATHY

Top 5 symptoms//phenotypes associated to Congestive heart failure and Eosinophilia

Symptoms // Phenotype % cases
Fatigue Common - Between 50% and 80% cases
Fever Uncommon - Between 30% and 50% cases
Seizures Uncommon - Between 30% and 50% cases
Leukocytosis Uncommon - Between 30% and 50% cases
Abdominal pain Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

Patients with Congestive heart failure and Eosinophilia. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases


Thrombocytopenia Headache Hepatomegaly Cardiomyopathy Lymphadenopathy Arthritis Edema Splenomegaly Cataract Arrhythmia Strabismus Growth delay Dyspnea Hepatosplenomegaly Meningitis Pain Global developmental delay Short stature Scoliosis Cognitive impairment Uveitis Osteolysis Erythema Pulmonary arterial hypertension Intellectual disability Ptosis Osteopenia Myopia Myopathy Portal hypertension Dilatation Interstitial pulmonary abnormality Failure to thrive Sensorineural hearing impairment Syncope

Rare Symptoms - Less than 30% cases


Hepatic fibrosis Increased antibody level in blood Verrucae Osteoporosis Feeding difficulties Abnormality of skin pigmentation Hepatocellular carcinoma Jaundice Elevated erythrocyte sedimentation rate Cholestasis Tubulointerstitial nephritis Cholelithiasis Recurrent pharyngitis Cirrhosis Ascites Hepatitis Depressivity Inflammation of the large intestine Bruising susceptibility Decreased liver function Elevated serum creatine phosphokinase Pancytopenia Cough Palpitations Scarring Bronchiectasis Anorexia Proximal muscle weakness Elevated hepatic transaminase Abdominal distention Weight loss Renal insufficiency Abnormality of the liver Leukopenia Dilated cardiomyopathy Anemia Pleural effusion Abnormal bleeding Immunodeficiency Corneal opacity Hypoalbuminemia Tachypnea Abnormal myocardium morphology Respiratory distress Diarrhea Synovitis Osteomyelitis Hypertension Glaucoma Motor delay Spasticity Visual impairment Muscular hypotonia Muscle weakness Hypertrophic cardiomyopathy Alopecia Neoplasm Abnormality of bone marrow cell morphology Respiratory tract infection Skin rash Recurrent upper respiratory tract infections Nystagmus Stroke Proteinuria Hematuria Arthralgia Apraxia Migraine Oculomotor apraxia Spastic paraparesis Irritability Epistaxis Nausea and vomiting Increased bone mineral density Progressive neurologic deterioration Osteoarthritis Decreased body weight Bone pain Clubbing Reduced bone mineral density Bipolar affective disorder Periorbital edema Generalized osteosclerosis Abnormality of the spleen Avascular necrosis of the capital femoral epiphysis Multiple myeloma Supranuclear gaze palsy Vertebral compression fractures Edema of the lower limbs Increased serum ferritin Gingival bleeding Increased susceptibility to fractures Protuberant abdomen Aseptic necrosis Exertional dyspnea Pathologic fracture Pericardial effusion Petechiae Abnormality of coagulation Menorrhagia Abnormality of the thorax Abnormality of the cardiovascular system Abnormality of nail color Myocardial infarction CSF pleocytosis Abnormal oral mucosa morphology EEG abnormality Myoclonus Glossitis Arteritis Abnormal pericardium morphology Conjunctival hyperemia Dementia Recurrent respiratory infections Hypersplenism Cervical lymphadenopathy Ascending tubular aorta aneurysm Delayed skeletal maturation Kyphosis Ataxia Abnormal gallbladder morphology Aseptic leukocyturia Coronary artery aneurysm Strawberry tongue Double outlet right ventricle with subpulmonary ventricular septal defect without pulmonary stenosis Abnormal emotion/affect behavior Pyuria Cholecystitis Abnormality of the eye Mitral regurgitation Pericarditis Vasculitis Conjunctivitis Arthralgia/arthritis Cranial nerve paralysis Ischemic stroke Cyanosis Scaling skin Hyponatremia Coronary artery atherosclerosis Abnormal heart valve morphology Acute kidney injury Neurological speech impairment Parkinsonism Aortic root aneurysm Myocarditis Generalized myoclonic seizures Allergy Inflammatory abnormality of the eye Elevated C-reactive protein level Cheilitis Abnormality of eye movement Delayed puberty Esodeviation Short neck Fractures of the long bones Abnormality of color vision Restrictive cardiomyopathy Atrial flutter Nonimmune hydrops fetalis Drusen Malignant hyperthermia Arnold-Chiari type I malformation Gonadal dysgenesis Abnormality of blood and blood-forming tissues Neuroblastoma Abnormality of the vertebral column Male infertility Cystic hygroma Neurofibromas Abnormality of the coagulation cascade Schwannoma Radial deviation of finger Cubitus valgus Myelodysplasia Patent foramen ovale Failure to thrive in infancy Elevated alkaline phosphatase Pterygium Poor suck Arnold-Chiari malformation Bicuspid aortic valve Azoospermia Plagiocephaly Lymphedema Shield chest Multiple lentigines Left ventricular hypertrophy Preductal coarctation of the aorta Impaired myocardial contractility Abnormality of neutrophils Abnormal left ventricle morphology Severe sensorineural hearing impairment Thromboembolism Lipoatrophy Congenital sensorineural hearing impairment Palmoplantar hyperkeratosis Ventricular arrhythmia EMG abnormality Palmoplantar keratoderma Ventriculomegaly Postductal coarctation of the aorta Nasogastric tube feeding Asymmetry of the thorax Reduced factor XIII activity Gonadal neoplasm Pectus excavatum of inferior sternum Loose anagen hair Juvenile myelomonocytic leukemia Panuveitis Neurofibrosarcoma Reduced factor XII activity Superior pectus carinatum Amegakaryocytic thrombocytopenia Hypoplastic aortic arch Lymphangioma Optic disc hypoplasia Amblyopia Clumsiness Spontaneous hematomas Micrognathia Intellectual disability, mild Vomiting Atrial septal defect Bone marrow hypercellularity Ventricular septal defect Downslanted palpebral fissures Brachydactyly Epicanthus Depressed nasal bridge High palate Low-set ears Cryptorchidism Abnormal facial shape Hypertelorism Hernia Microcephaly Horizontal supranuclear gaze palsy Cardiac valve calcification Hematological neoplasm Decreased beta-glucocerebrosidase protein and activity Puberty and gonadal disorders Biliary tract obstruction Vascular calcification Erlenmeyer flask deformity of the femurs Orthopnea Abnormal platelet function Arthralgia of the hip Flank pain Abnormality of cardiovascular system morphology Pectus excavatum Primary amenorrhea Broad forehead Low posterior hairline Ventricular hypertrophy Coarctation of aorta Amenorrhea Wide intermamillary distance Webbed neck Dental malocclusion Triangular face High, narrow palate Facial asymmetry Pulmonic stenosis Hypotrichosis Leukemia Abnormal cardiac septum morphology Clinodactyly Sparse hair Postnatal growth retardation Low-set, posteriorly rotated ears Kyphoscoliosis Gastroesophageal reflux Polyhydramnios Proptosis Hypogonadism Posteriorly rotated ears Rod-cone dystrophy Constipation Abnormal heart morphology Patent ductus arteriosus Myelokathexis Histiocytosis Hypersegmentation of neutrophil nuclei Hypoplastic fingernail Retinal vascular proliferation Broad nail Abnormal hand morphology Ridged fingernail Abnormal chorioretinal morphology Absent hand Retinal hemorrhage Asymmetric growth Supernumerary ribs Deviation of finger Cerebral ischemia Dystrophic toenail Skeletal muscle atrophy Abnormal toenail morphology Hearing abnormality Irregular hyperpigmentation Abnormality of immune system physiology Telangiectasia of the skin Supernumerary nipple Hemiplegia/hemiparesis Keratitis Abnormality of dental morphology Encephalitis Hypopigmented skin patches Peripheral neuropathy Blindness Abnormality of the fingernails Ventricular tachycardia Hyperuricemia Hyperthyroidism Abnormality of the musculature Chorioretinal atrophy Blurred vision Pulmonary fibrosis Emphysema Diabetes insipidus Epiphora Hypercalcemia Hypercalciuria Nephrocalcinosis Hypothyroidism Hyperpigmentation of the skin Nephrolithiasis Subcutaneous nodule Abnormal lung morphology Sudden cardiac death Chest pain Hypopigmentation of the skin Hemolytic anemia Hepatic failure Papule Facial palsy Photophobia Spina bifida occulta Abnormality of dental enamel Hemoptysis Cardiac arrest Cardiorespiratory arrest Meningocele Mitochondrial myopathy Hypoplasia of the brainstem Abnormality of mitochondrial metabolism Premature ovarian insufficiency Abnormal electroretinogram Easy fatigability Ragged-red muscle fibers Corneal dystrophy Exercise intolerance Hemiparesis Organic aciduria Esotropia Aciduria Increased serum lactate Generalized muscle weakness Lactic acidosis Congenital cataract Feeding difficulties in infancy Mental deterioration Acidosis Cerebellar hypoplasia Respiratory insufficiency Generalized hypotonia Right ventricular hypertrophy Skeletal myopathy Abnormality of the nail Umbilical hernia Abnormality of the hair Skin ulcer Blue sclerae Abnormal blistering of the skin Hypodontia Delayed eruption of teeth Retinal detachment Oral cleft Finger syndactyly Attention deficit hyperactivity disorder Camptodactyly of finger Hyperkeratosis 3-Methylglutaconic aciduria Cerebral cortical atrophy Hyperhidrosis Microphthalmia Gait disturbance Depletion of mitochondrial DNA in muscle tissue Abnormal muscle fiber protein expression Exercise-induced lactic acidemia Infantile axial hypotonia Inferior vermis hypoplasia Fatty replacement of skeletal muscle Decreased activity of mitochondrial respiratory chain Abnormal myelination Keratoconjunctivitis sicca Optic neuropathy Tonsillitis Prolonged prothrombin time Elevated alkaline phosphatase of hepatic origin Palmar telangiectasia Abnormal biliary tract morphology Chronic hepatic failure Vitamin K deficiency Vitamin A deficiency Cholangiocarcinoma Vitamin E deficiency Sclerosing cholangitis Abnormal eosinophil morphology Vitamin D deficiency Cholangitis Spider hemangioma Cholestatic liver disease Ulcerative colitis Acute hepatic failure Thyroiditis Amyloidosis Celiac disease Abnormality of the thyroid gland Generalized amyotrophy Pancreatitis Type I diabetes mellitus Pruritus Polyclonal elevation of IgM Abnormal large intestine physiology Encephalopathy Sinusitis Septic arthritis Folliculitis Abnormality of female external genitalia Abnormality of female internal genitalia Atelectasis B-cell lymphoma Periodontitis IgG deficiency Cellulitis Combined immunodeficiency Recurrent bacterial infections Recurrent urinary tract infections Neoplasm of the gallbladder Otitis media Decreased antibody level in blood Lymphoma Neutropenia Carious teeth Carcinoma Respiratory failure Pneumonia Hearing impairment Adenocarcinoma of the large intestine Dilated superficial abdominal veins Recurrent systemic pyogenic infections Autoimmunity Pharyngitis Joint swelling Vitreous hemorrhage Anterior uveitis Dacryocystitis Chorioretinitis Abnormality of the adrenal glands Abnormality of the lymph nodes Skin plaque Generalized lymphadenopathy Erythema nodosum Abnormality of the cerebrospinal fluid Cystoid macular edema Chylothorax Abnormality of the pleura Iridocyclitis Pneumothorax Anterior synechiae of the anterior chamber Night sweats Skin nodule Bone cyst Immune dysregulation Macular edema Upper airway obstruction Abnormality of the gastrointestinal tract Hypothermia Increased CSF protein Heart block Abnormal salivary gland morphology Abnormal conjunctiva morphology Gastrointestinal inflammation Enlarged lacrimal glands Pyelonephritis Severe failure to thrive Progressive proximal muscle weakness Psoriasiform dermatitis Progressive muscle weakness Eczema Myalgia Recurrent infections Abnormal trabecular meshwork morphology Pulmonary granulomatosis Vitreous snowballs Maculopapular exanthema Vitreous floaters Abnormality of the nasal mucosa Increased T cell count Abnormal cardiac ventricular function Parotitis Abnormal liver parenchyma morphology Non-caseating epithelioid cell granulomatosis Abnormality of T cell physiology Enlargement of parotid gland Posterior vitreous detachment Abnormality of skin morphology Abnormal reproductive system morphology Vitritis Diffuse palmoplantar hyperkeratosis



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