Congestive heart failure, and Bronchiectasis

Diseases related with Congestive heart failure and Bronchiectasis

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


Top matches:

High match IDIOPATHIC PULMONARY FIBROSIS


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

High 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

High match COMBINED IMMUNODEFICIENCY DUE TO LRBA DEFICIENCY


Common variable immunodeficiency-8 with autoimmunity is an autosomal recessive disorder of immune dysregulation. Affected individuals have early childhood onset of recurrent infections, particularly respiratory infections, and also develop variable autoimmune disorders, including idiopathic thrombocytopenic purpura, autoimmune hemolytic anemia, and inflammatory bowel disease. The presentation and phenotype are highly variable, even within families (summary by Lopez-Herrera et al., 2012 and Alangari et al., 2012). Immunologic findings are also variable and may include decreased B cells, hypogammaglobulinemia, and deficiency of CD4+ T regulatory (Treg) cells (Charbonnier et al., 2015).For a general description and a discussion of genetic heterogeneity of common variable immunodeficiency, see CVID1 (OMIM ).

COMBINED IMMUNODEFICIENCY DUE TO LRBA DEFICIENCY Is also known as cid due to lrba deficiency

Related symptoms:

  • Growth delay
  • Neoplasm
  • Failure to thrive
  • Anemia
  • Diarrhea


SOURCES: OMIM ORPHANET MENDELIAN

More info about COMBINED IMMUNODEFICIENCY DUE TO LRBA DEFICIENCY

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Other less relevant matches:

High match AUTOIMMUNE ENTEROPATHY AND ENDOCRINOPATHY-SUSCEPTIBILITY TO CHRONIC INFECTIONS SYNDROME


Autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome is an extremely rare, autosomal dominant immunological disorder characterized by variable enteropathy, endocrine disorders (e.g. type 1 diabetes mellitus, hypothyroidism), immune dysregulation with pulmonary and blood-borne bacterial infections, and fungal infections (chronic mucocutaneous candidiasis) developing in infancy. Other manifestations include short stature, eczema, hepatosplenomegaly, delayed puberty, and osteoporosis/osteopenia.

AUTOIMMUNE ENTEROPATHY AND ENDOCRINOPATHY-SUSCEPTIBILITY TO CHRONIC INFECTIONS SYNDROME Is also known as candf7|candidiasis, familial, 7|candidiasis, familial chronic mucocutaneous, autosomal dominant

Related symptoms:

  • Global developmental delay
  • Short stature
  • Growth delay
  • Anemia
  • Diarrhea


SOURCES: ORPHANET OMIM MENDELIAN

More info about AUTOIMMUNE ENTEROPATHY AND ENDOCRINOPATHY-SUSCEPTIBILITY TO CHRONIC INFECTIONS SYNDROME

High 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

Low match MUCOPOLYSACCHARIDOSIS, TYPE II; MPS2


Mucopolysaccharidosis II is a rare X-linked recessive disorder caused by deficiency of the lysosomal enzyme iduronate sulfatase, leading to progressive accumulation of glycosaminoglucans in nearly all cell types, tissues, and organs. Patients with MPS II excrete excessive amounts of chondroitin sulfate B (dermatan sulfate) and heparitin sulfate (heparan sulfate) in the urine (McKusick, 1972; Wraith et al., 2008).

MUCOPOLYSACCHARIDOSIS, TYPE II; MPS2 Is also known as hunter syndrome|sulfoiduronate sulfatase deficiency|sids deficiency|mps ii|ids deficiency|iduronate 2-sulfatase deficiency

Related symptoms:

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


SOURCES: OMIM MENDELIAN

More info about MUCOPOLYSACCHARIDOSIS, TYPE II; MPS2

Low match MUCOLIPIDOSIS TYPE II


Mucolipidosis II (MLII) is a slowly progressive lysosomal disorder characterized by growth retardation, skeletal abnormalities, facial dysmorphism, stiff skin, developmental delay and cardiomegaly.

MUCOLIPIDOSIS TYPE II Is also known as i-cell disease|ml ii|mucolipidosis ii|n-acetylglucosamine 1-phosphotransferase deficiency|mucolipidosis type ii alpha/beta|ml ii alpha/beta|icd

Related symptoms:

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


SOURCES: ORPHANET OMIM MESH MENDELIAN

More info about MUCOLIPIDOSIS TYPE II

Low match ALSTRÖM SYNDROME


Alström syndrome (AS) is a multisystemic disorder characterized by cone-rod dystrophy, hearing loss, obesity, insulin resistance and hyperinsulinemia, type 2 diabetes mellitus, dilated cardiomyopathy (DCM; see this term), and progressive hepatic and renal dysfunction.

ALSTRÖM SYNDROME Is also known as alss

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Hearing impairment


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about ALSTRÖM SYNDROME

Low match HYPOHIDROTIC ECTODERMAL DYSPLASIA WITH IMMUNODEFICIENCY


Hypohidrotic ectodermal dysplasia with immunodeficiency (HED-ID) is a type of HED (see this term) characterized by the malformation of ectodermal structures such as skin, hair, teeth and sweat glands, and associated with immunodeficiency.

HYPOHIDROTIC ECTODERMAL DYSPLASIA WITH IMMUNODEFICIENCY Is also known as hed-id|anhidrotic ectodermal dysplasia with immunodeficiency|eda-id

Related symptoms:

  • Failure to thrive
  • Diarrhea
  • Immunodeficiency
  • Recurrent infections
  • Pneumonia


SOURCES: ORPHANET OMIM MENDELIAN

More info about HYPOHIDROTIC ECTODERMAL DYSPLASIA WITH IMMUNODEFICIENCY

Low match ALPHA-1-ANTITRYPSIN DEFICIENCY


Alpha-1-antitrypsin deficiency is a hereditary disease that develops in adulthood and is characterized by chronic liver disorders (cirrhosis), respiratory disorders (emphysema), and rarely panniculitis.

ALPHA-1-ANTITRYPSIN DEFICIENCY Is also known as deficiency in alpa-1-proteinase inhibitor

Related symptoms:

  • Neoplasm
  • Hypertension
  • Hepatomegaly
  • Fatigue
  • Respiratory distress


SOURCES: ORPHANET MESH OMIM MENDELIAN

More info about ALPHA-1-ANTITRYPSIN DEFICIENCY

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

Symptoms // Phenotype % cases
Pneumonia Common - Between 50% and 80% cases
Splenomegaly Uncommon - Between 30% and 50% cases
Respiratory tract infection Uncommon - Between 30% and 50% cases
Hepatomegaly Uncommon - Between 30% and 50% cases
Neoplasm Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases


Growth delay Immunodeficiency Failure to thrive Diarrhea Recurrent respiratory infections Hypothyroidism Hepatosplenomegaly Recurrent upper respiratory tract infections Weight loss Recurrent otitis media Abnormal lung morphology Seizures Respiratory distress Respiratory failure Dyspnea Carcinoma Global developmental delay Asthma Anemia Cardiomyopathy Intellectual disability Emphysema Portal hypertension Immune dysregulation Osteopenia Fatigue Blindness Hemolytic anemia Visual impairment Recurrent infections Thrombocytopenia Inflammation of the large intestine Diabetes mellitus Autoimmune thrombocytopenia Hepatic failure Lymphadenopathy Hepatitis Kyphosis Short stature Cough Pulmonary arterial hypertension Hypertension Arthritis Cirrhosis Hearing impairment Scarring Otitis media Interstitial pulmonary abnormality Fever Pulmonary fibrosis

Rare Symptoms - Less than 30% cases


Photophobia Alopecia Recurrent pneumonia Thickened skin Cardiomegaly Abnormality of the liver Jaundice Renal insufficiency Generalized hirsutism Elevated hepatic transaminase Peripheral neuropathy Cataract Pain Renovascular hypertension Pericardial effusion Delayed puberty Recurrent bronchitis Dilatation Anorexia Retinopathy Retinal degeneration Hyperuricemia Coarse facial features Macroglossia Rod-cone dystrophy Severe short stature Inguinal hernia Pigmentary retinopathy Short neck Cognitive impairment Split hand Tubulointerstitial nephritis Hemoptysis Chorioretinal atrophy Umbilical hernia Abnormality of retinal pigmentation Hoarse voice Chronic obstructive pulmonary disease Nephrocalcinosis Decreased liver function Hyperpigmentation of the skin Aortic regurgitation Corneal dystrophy Abnormal heart valve morphology Dysostosis multiplex Myelopathy Urinary glycosaminoglycan excretion Ataxia Diabetes insipidus Generalized lymphadenopathy Abnormal intestine morphology Gastroesophageal reflux Cyanosis Lymphoma Pulmonary insufficiency Carious teeth Clubbing Increased antibody level in blood Autoimmune hemolytic anemia Purpura Recurrent urinary tract infections Type I diabetes mellitus Chronic diarrhea Inflammatory abnormality of the skin Clubbing of fingers Pancytopenia Abnormality of female external genitalia Autoimmunity Verrucae Decreased antibody level in blood Neutropenia Sinusitis Villous atrophy Respiratory insufficiency Combined immunodeficiency Atherosclerosis Abnormality of renal calyx morphology Abnormality of prothrombin Type II diabetes mellitus Optic disc pallor Hypohidrotic ectodermal dysplasia Goiter EEG with occipital slowing Specific learning disability Progressive visual loss Decreased testicular size Intractable diarrhea Localized hirsutism Polycystic ovaries Dysgammaglobulinemia Growth hormone deficiency Abnormality of the hand Precocious puberty in females Gastrointestinal hemorrhage Round face Nephrotic syndrome Urinary incontinence Vesicoureteral reflux Abdominal distention Epidermal acanthosis Recurrent skin infections Anhidrotic ectodermal dysplasia Short toe Macular degeneration Accelerated skeletal maturation Absence seizures Hyperlipidemia Hypogonadotrophic hypogonadism Increased body weight Horizontal nystagmus Hypergonadotropic hypogonadism Pancreatitis Hypercholesterolemia Gynecomastia Hypertriglyceridemia Tachypnea Ectodermal dysplasia Abnormality of the femoral head Hepatic fibrosis Vitreous haze Insulin resistance Left ventricular hypertrophy Cone/cone-rod dystrophy Involuntary movements Acanthosis nigricans Ascites Stage 5 chronic kidney disease Sleep disturbance Encephalopathy Autism Hyperkeratosis Polydactyly Abdominal pain Hypogonadism Hyperhidrosis Myoclonus Constipation Hyporeflexia Patent ductus arteriosus Visual loss Clinodactyly Depressivity Pes planus Obesity Dystonia Behavioral abnormality Abnormality of the dentition Vomiting Optic atrophy Motor delay Delayed speech and language development Feeding difficulties Sensorineural hearing impairment Strabismus Nystagmus Scoliosis Kyphoscoliosis Deeply set eye Nephropathy Generalized tonic-clonic seizures Hepatic steatosis Retinal dystrophy Hirsutism Cholestasis Tachycardia Nausea Dry skin Infertility Pulmonic stenosis Ophthalmoplegia Hypermetropia Hypotrichosis Dilated cardiomyopathy Neoplasm of the liver Nyctalopia Sparse hair Vasculitis Autistic behavior Wheezing Pallor Hepatocellular carcinoma Postnatal growth retardation Irritability Abnormality of the kidney Proteinuria Myalgia Conductive hearing impairment Cholelithiasis Polydipsia Elevated alkaline phosphatase Urinary retention Hepatic encephalopathy Urethral stenosis Achromatopsia Acute pancreatitis Increased circulating androgen level Exudative retinopathy Nonproductive cough Abnormal adipose tissue morphology Chronic active hepatitis Chills Pyelonephritis Hyperostosis frontalis interna Poor fine motor coordination Arteriosclerosis Bull's eye maculopathy Elevated C-reactive protein level Tubulointerstitial fibrosis Testicular atrophy Abnormal left ventricle morphology Abnormal renal physiology Disinhibition Retinal pigment epithelial atrophy Endocardial fibroelastosis Abnormal renal morphology Menstrual irregularities Decreased HDL cholesterol concentration Receptive language delay Granular macular appearance Multinodular goiter Vertical nystagmus Ovarian cyst Urethral stricture Hypoplastic male external genitalia Chronic hepatic failure Facial hirsutism ST segment depression Abnormality of the pituitary gland Multifocal atrial tachycardia Childhood-onset truncal obesity Urethral obstruction Squared iliac bones Albuminuria Abnormal muscle tone Female hypogonadism Impaired temperature sensation Abnormal chorioretinal morphology Increased total bilirubin Epigastric pain Abnormality of dental color Lumbar scoliosis Abnormality of the urethra Chronic infection Abnormal spermatogenesis Decreased glomerular filtration rate Abnormality of the optic disc First degree atrioventricular block Melena High-frequency sensorineural hearing impairment Hematemesis Frontal balding Thickened ears High-frequency hearing impairment Precocious puberty Hydroureter Pericarditis Subcapsular cataract Increased number of teeth Bronchitis Glycosuria Glomerulopathy Progressive sensorineural hearing impairment Agenesis of permanent teeth Short finger Polyphagia Abnormal retinal morphology Truncal obesity Urinary urgency Polyuria Severe sensorineural hearing impairment Glucose intolerance Hyperglycemia Hyperostosis Acne Impaired vibratory sensation Constriction of peripheral visual field Aplasia/Hypoplasia of the cerebellum Obsessive-compulsive behavior Chronic otitis media Nephritis Hepatic necrosis Lipodystrophy Hyperinsulinemia Thoracic scoliosis Hypoventilation Restrictive cardiomyopathy Elevated serum creatinine Esophageal varix Dilatation of the bladder Chronic fatigue Unilateral breast hypoplasia Myocardial fibrosis Male hypogonadism Beaking of vertebral bodies T12-L3 Glue ear Oligospermia Recurrent cystitis Myocarditis Tubular atrophy Acute hepatic failure Widely-spaced incisors Insulin-resistant diabetes mellitus Right ventricular hypertrophy Attenuation of retinal blood vessels Pendular nystagmus Gingivitis Ketoacidosis Broad foot Abnormal retinal artery morphology Posterior subcapsular cataract Oligomenorrhea Poor coordination Hyperventilation Alopecia of scalp Peripheral visual field loss Retinal atrophy Lower thoracic interpediculate narrowness Talipes equinovarus Varus deformity of humeral neck Proximal muscle weakness Leukopenia Osteolysis Nephrolithiasis Subcutaneous nodule Palpitations Syncope Sudden cardiac death Chest pain Hypopigmentation of the skin Papule Erythema Facial palsy Glaucoma Eosinophilia Arrhythmia Headache Edema Skeletal muscle atrophy Abnormal serum interferon-gamma level Medial calcification of large arteries Esophageal carcinoma Oropharyngeal squamous cell carcinoma Susceptibility to herpesvirus Recurrent Aspergillus infections Carotid artery dilatation Functional abnormality of the bladder Autoimmune neutropenia Ventricular tachycardia Hypercalciuria Antiphospholipid antibody positivity Upper airway obstruction Erythema nodosum Abnormality of the cerebrospinal fluid Cystoid macular edema Chylothorax Vitreous hemorrhage Abnormality of the pleura Pneumothorax Anterior synechiae of the anterior chamber Night sweats Skin nodule Bone cyst Macular edema Abnormality of the gastrointestinal tract Hypercalcemia Hypothermia Increased CSF protein Heart block Joint swelling Uveitis Optic neuropathy Keratoconjunctivitis sicca Hyperthyroidism Abnormality of the musculature Elevated erythrocyte sedimentation rate Blurred vision Epiphora Pleural effusion Renal artery stenosis B lymphocytopenia Abnormality of the lymph nodes Osteomyelitis Bone marrow hypercellularity Hypersegmentation of neutrophil nuclei Tonsillitis Septic arthritis Folliculitis Abnormality of bone marrow cell morphology Abnormality of female internal genitalia Atelectasis B-cell lymphoma Periodontitis IgG deficiency Cellulitis Leukocytosis Conjunctivitis Recurrent bacterial infections Meningitis Ground-glass opacification on pulmonary HRCT Honeycomb lung Reticular pattern on pulmonary HRCT Hypocapnia Alveolar cell carcinoma Crackles Right ventricular failure Pulmonary infiltrates Polycythemia Exertional dyspnea Scaling skin Myelokathexis Colitis Primary hypothyroidism Lymphopenia Decrease in T cell count Enterocolitis Generalized osteoporosis Chronic mucocutaneous candidiasis Abnormality of the endocrine system Dilatation of the cerebral artery Hashimoto thyroiditis Pulmonary embolism Thyroiditis Patent foramen ovale Encephalitis Leukoencephalopathy Eczema Recurrent sinusitis Sepsis Delayed skeletal maturation Burkitt lymphoma Follicular hyperplasia Interstitial pneumonitis Gastritis IgM deficiency Cor pulmonale Brain neoplasm Chronic lung disease Exocrine pancreatic insufficiency Fatigable weakness IgA deficiency Skin plaque Abnormality of the adrenal glands Progressive alveolar ridge hypertropy Short palm Abnormality of the thorax Metaphyseal widening Short long bone Opacification of the corneal stroma Congenital hip dislocation Sparse and thin eyebrow Gingival overgrowth Thin skin Narrow forehead Hip dysplasia Wide intermamillary distance Brain atrophy Severe global developmental delay Flared metaphysis Hip dislocation Joint stiffness Joint laxity Hypertrophic cardiomyopathy Neonatal hypotonia High forehead Hernia Long philtrum Anteverted nares Abnormality of the skeletal system Epicanthus Depressed nasal bridge Abnormal facial shape Heart murmur Pathologic fracture Dermatan sulfate excretion in urine Abnormality of the rib cage Bullet-shaped phalanges of the hand Deficiency of N-acetylglucosamine-1-phosphotransferase Increased serum iduronate sulfatase activity Increased serum beta-hexosaminidase Thoracolumbar kyphoscoliosis Atlantoaxial dislocation Large sella turcica Broad alveolar ridges Cavernous hemangioma Mucopolysacchariduria Abnormality of nervous system morphology Carpal bone hypoplasia Flared iliac wings Vertebral fusion Lack of skin elasticity Ovoid vertebral bodies Hypoplastic scapulae Flat acetabular roof Corneal erosion Diastasis recti Radial bowing Severe postnatal growth retardation Megalocornea Protuberant abdomen Palpebral edema Hypoplasia of the odontoid process Thickened calvaria Generalized hypotonia Retinoschisis Chorioretinitis Parotitis Hydrocephalus Macrocephaly Flexion contracture Ptosis Abnormal trabecular meshwork morphology Pulmonary granulomatosis Vitreous snowballs Enlarged lacrimal glands Maculopapular exanthema Abnormality of the nasal mucosa Increased T cell count Abnormal cardiac ventricular function Abnormal liver parenchyma morphology Apnea 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 Vitreous floaters Abnormal conjunctiva morphology Iridocyclitis Abnormal salivary gland morphology Anterior uveitis Dacryocystitis Pes cavus Attention deficit hyperactivity disorder Tracheobronchomalacia Intellectual disability, progressive Cervical cord compression Heparan sulfate excretion in urine Retinal fold Intestinal pseudo-obstruction Obstructive sleep apnea Papilledema Scaphocephaly Mild short stature Incoordination Sleep apnea Widely spaced teeth Spastic tetraparesis Exercise intolerance Corneal opacity Elbow flexion contracture Progressive neurologic deterioration Hypertrichosis Tetraparesis Thick lower lip vermilion Intellectual disability, profound Spastic tetraplegia Tetraplegia Postural instability Delayed eruption of teeth Neurodegeneration Abnormality of the cerebral white matter Dolichocephaly Panniculitis



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