Hypertension, and Bronchiectasis

Diseases related with Hypertension and Bronchiectasis

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

Top matches:

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

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

Medium match CYSTIC FIBROSIS

Cystic fibrosis (CF) is a genetic disorder characterized by the production of sweat with a high salt content and mucus secretions with an abnormal viscosity.

CYSTIC FIBROSIS Is also known as mucoviscidosis|cf

Related symptoms:

  • Growth delay
  • Neoplasm
  • Failure to thrive
  • Pain
  • Hypertension


SOURCES: ORPHANET OMIM MENDELIAN

More info about CYSTIC FIBROSIS

Other less relevant matches:

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

Related symptoms:

  • Global developmental delay
  • Hearing impairment
  • Microcephaly
  • Growth delay
  • Failure to thrive


SOURCES: ORPHANET OMIM MENDELIAN

More info about NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4

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

Cartilage-hair hypoplasia is a disease affecting the bone metaphyses causing small stature from birth.

CARTILAGE-HAIR HYPOPLASIA Is also known as autosomal recessive metaphyseal chondrodysplasia|metaphyseal chondrodysplasia, mckusick type

Related symptoms:

  • Intellectual disability
  • Short stature
  • Scoliosis
  • Growth delay
  • Neoplasm


SOURCES: OMIM ORPHANET MENDELIAN

More info about CARTILAGE-HAIR HYPOPLASIA

Deficiency in anterior pituitary function-variable immunodeficiency syndrome is a rare, genetic endocrine disease characterized by the association of common variable immunodeficiency, manifesting with hypogammaglobulinemia and recurrent or severe childhood-onset sinopulmonary infections, followed, possibly many years later, by symptomatic adrenocorticotropic hormone (ACTH) deficiency resulting from anterior pituitary hormone deficiency.

DEFICIENCY IN ANTERIOR PITUITARY FUNCTION-VARIABLE IMMUNODEFICIENCY SYNDROME Is also known as david syndrome

Related symptoms:

  • Global developmental delay
  • Failure to thrive
  • Fatigue
  • Alopecia
  • Nail dystrophy


SOURCES: ORPHANET MENDELIAN

More info about DEFICIENCY IN ANTERIOR PITUITARY FUNCTION-VARIABLE IMMUNODEFICIENCY SYNDROME

Related symptoms:

  • Failure to thrive
  • Hypertension
  • Respiratory distress
  • Edema
  • Vomiting


SOURCES: OMIM MENDELIAN

More info about INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL, 2; NISBD2

Low match KEUTEL SYNDROME

Keutel syndrome is characterised by diffuse cartilage calcification, brachytelephalangism, peripheral pulmonary artery stenoses and facial dysmorphism.

KEUTEL SYNDROME Is also known as pulmonic stenosis-brachytelephalangism-calcification of cartilages syndrome|pulmonic stenosis, brachytelephalangism, and calcification of cartilages

Related symptoms:

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


SOURCES: OMIM MESH ORPHANET MENDELIAN

More info about KEUTEL SYNDROME

Top 5 symptoms//phenotypes associated to Hypertension and Bronchiectasis

Symptoms // Phenotype % cases
Respiratory distress Common - Between 50% and 80% cases
Carcinoma Common - Between 50% and 80% cases
Failure to thrive Uncommon - Between 30% and 50% cases
Hepatomegaly Uncommon - Between 30% and 50% cases
Neoplasm Uncommon - Between 30% and 50% cases

Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases

Diarrhea Portal hypertension Emphysema Alopecia Growth delay Abnormal lung morphology Pulmonary arterial hypertension Pneumonia Global developmental delay Recurrent infections Recurrent respiratory infections Thrombocytopenia Anemia Dilatation Splenomegaly Recurrent upper respiratory tract infections Decreased antibody level in blood Asthma Immunodeficiency Hemoptysis Chronic obstructive pulmonary disease Lymphopenia Short stature Sepsis Fatigue Recurrent pneumonia Pulmonary fibrosis Cirrhosis Cough Respiratory insufficiency Scarring Congestive heart failure Respiratory failure Dyspnea Respiratory tract infection

Rare Symptoms - Less than 30% cases

Hepatosplenomegaly Hemolytic anemia Macrotia Depressed nasal bridge Hypothyroidism Delayed skeletal maturation Postural instability Obstructive lung disease Intellectual disability Pneumothorax Abnormality of the pancreas Exocrine pancreatic insufficiency Hypotrichosis Neutropenia Pulmonic stenosis Immune dysregulation Pectus carinatum Bronchiolitis Leukopenia Joint laxity Hypercalciuria Midface retrusion Cutis laxa Wide nasal bridge Hearing impairment Recurrent sinusitis Heart block Autoimmune thrombocytopenia Seizures Visual impairment Edema Thyroiditis Papule Recurrent bronchitis Hypopigmentation of the skin Inflammation of the large intestine Hydronephrosis Recurrent otitis media Wheezing Dehydration Delayed puberty Malabsorption Diabetes mellitus Hepatic failure Abnormality of the liver Vomiting Elevated hepatic transaminase Pain Clubbing Increased antibody level in blood Weight loss Hepatitis Infertility Fever Interstitial pulmonary abnormality Nephrocalcinosis Gastroesophageal reflux Sinusitis Disproportionate short-limb short stature Short ribs Squamous cell carcinoma Cone-shaped epiphysis Hypocalcemia Sparse eyelashes Metaphyseal widening Neoplasm of the skin Accelerated skeletal maturation Calcification of the auricular cartilage Abnormal palate morphology Reduced tendon reflexes Genu varum Costal cartilage calcification Sacral dimple Abnormality of pelvic girdle bone morphology Limited elbow extension Short thorax Hodgkin lymphoma Generalized joint laxity Tracheal stenosis Fair hair Upper limb undergrowth Overweight Thrombocytosis Distal arthrogryposis Esophageal atresia Hypoplasia of the odontoid process Anal stenosis Macrocytic anemia Mesomelia Arterial calcification Metaphyseal dysplasia Calcification of cartilage High hypermetropia Abnormality of the hip bone Tracheal atresia Tibial bowing Basal cell carcinoma Gingival overgrowth Femoral bowing Soft, doughy skin Sparse and thin eyebrow Progressive hearing impairment Abnormality of retinal pigmentation Short neck Low-set, posteriorly rotated ears EEG abnormality Skeletal dysplasia Premature fusion of phalangeal epiphyses Brachycephaly Prominent forehead Severe short stature Constipation Cardiomyopathy Anteverted nares Sparse hair Abnormality of the skeletal system Myopia Epicanthus Cognitive impairment Muscular hypotonia Strabismus Scoliosis Abnormal trabecular meshwork morphology Pulmonary granulomatosis Vitreous snowballs Hyperlordosis Abnormal cardiac septum morphology Rhizomelia Abnormality of the ribs Abnormality of epiphysis morphology Aganglionic megacolon Bowing of the long bones Abnormal form of the vertebral bodies Abnormality of the metaphysis Aplastic anemia Depressed nasal ridge Fine hair Blue sclerae Lumbar hyperlordosis Convex nasal ridge Leukemia Gastrointestinal hemorrhage Lymphoma Small hand Short palm Joint hypermobility Micromelia Joint hyperflexibility Narrow chest Cartilaginous ossification of nose Arthrogryposis multiplex congenita B-cell lymphoma Papillary thyroid carcinoma Aplasia/Hypoplasia of the abdominal wall musculature Decreased serum insulin-like growth factor 1 Abnormality of the periungual region Severe B lymphocytopenia Abnormal size of pituitary gland Decreased circulating androgen level Abnormal lymphocyte morphology Dermal atrophy Nasal speech Aortic aneurysm Severe viral infections Adrenocorticotropin deficient adrenal insufficiency Epidermal acanthosis Hypoglycemic coma Mixed hearing impairment Decreased circulating ACTH level Recurrent pharyngitis Alopecia totalis Autoimmune antibody positivity Decreased circulating cortisol level Recurrent hypoglycemia Epiphyseal stippling Irregular vertebral endplates Coarctation of aorta Long eyelashes Vitiligo Growth abnormality Leukodystrophy Short thumb Short phalanx of finger Sloping forehead Cerebral calcification Memory impairment Otitis media Underdeveloped nasal alae Wide nose Short distal phalanx of finger Pustule Long face Osteoporosis Malar flattening Intellectual disability, mild Ventricular septal defect Optic atrophy Abnormal facial shape Deep philtrum Recurrent bronchiolitis Enlarged kidney Pulmonary artery stenosis Chronic sinusitis Aplasia/Hypoplasia affecting the eye Short nail Abnormal bone ossification Neonatal short-limb short stature Congenital hypoplastic anemia Spinal dysraphism Large face Hypersplenism Thyroid carcinoma Peripheral pulmonary artery stenosis Shortening of all distal phalanges of the fingers Normocytic anemia Hypoplastic anemia Mucopolysacchariduria Abnormal diaphysis morphology Diaphyseal thickening Spontaneous abortion Abnormality of chromosome stability Metaphyseal cupping Cellular immunodeficiency Abdominal aortic aneurysm Pulmonary artery hypoplasia Metaphyseal chondrodysplasia Abnormally ossified vertebrae Abnormal T cell morphology Hyperkalemia Susceptibility to chickenpox Hyponatremia Psoriasiform dermatitis Absence seizures Diplopia Short hallux Maculopapular exanthema Hypotension Growth hormone deficiency Nail dystrophy Pulmonary lymphoma Flaring of lower rib cage Abnormality of the distal phalanx of finger Absent pubertal growth spurt Abnormality of humoral immunity Biconvex vertebral bodies Severe T-cell immunodeficiency Sparse facial hair Impaired lymphocyte transformation with phytohemagglutinin Metaphyseal dysostosis Non-Hodgkin lymphoma Long fibula Narrow vertebral interpedicular distance Enlarged lacrimal glands Hyperthyroidism Abnormality of the nasal mucosa Leukoencephalopathy Villous atrophy Chronic mucocutaneous candidiasis Abnormality of the endocrine system Dilatation of the cerebral artery Hashimoto thyroiditis Pulmonary embolism Autoimmune hemolytic anemia Patent foramen ovale Encephalitis Abnormal intestine morphology Enterocolitis Purpura Type I diabetes mellitus Inflammatory abnormality of the skin Eczema Autoimmunity Osteopenia Microscopic nephrocalcinosis Echogenic fetal bowel Cellular metachromasia Biliary tract obstruction Generalized osteoporosis Decrease in T cell count Absent vas deferens Medial calcification of large arteries Hernia Kyphosis Atrial septal defect High palate Cryptorchidism Cleft palate Muscle weakness Sensorineural hearing impairment Microcephaly Abnormal serum interferon-gamma level Esophageal carcinoma Primary hypothyroidism Oropharyngeal squamous cell carcinoma Susceptibility to herpesvirus Recurrent Aspergillus infections Carotid artery dilatation Functional abnormality of the bladder Autoimmune neutropenia Renal artery stenosis Renovascular hypertension Antiphospholipid antibody positivity B lymphocytopenia Elevated sweat chloride Obstructive azoospermia Patent ductus arteriosus Reticular pattern on pulmonary HRCT Abdominal pain Panniculitis Neoplasm of the liver Hepatocellular carcinoma Vasculitis Cholestasis Nephrotic syndrome Jaundice Ground-glass opacification on pulmonary HRCT Honeycomb lung Hypocapnia Dyskinesia Alveolar cell carcinoma Crackles Pulmonary insufficiency Right ventricular failure Clubbing of fingers Pulmonary infiltrates Polycythemia Exertional dyspnea Scaling skin Cyanosis Nausea Abdominal distention Recurrent bronchopulmonary infections Allergy Meconium ileus Pancreatic adenocarcinoma Productive cough Secretory diarrhea Chronic pancreatitis Chronic infection Nasal polyposis Rectal prolapse Ileus Biliary cirrhosis Cor pulmonale Insulin resistance Chronic lung disease Neoplasm of the pancreas Bronchitis Male infertility Steatorrhea Malnutrition Intestinal obstruction Tachypnea Azoospermia Pancreatitis Clinodactyly Single transverse palmar crease Increased T cell count Increased CSF protein Abnormality of the pleura Anterior synechiae of the anterior chamber Night sweats Skin nodule Bone cyst Macular edema Upper airway obstruction Abnormality of the gastrointestinal tract Tubulointerstitial nephritis Hypothermia Joint swelling Chylothorax Uveitis Optic neuropathy Keratoconjunctivitis sicca Hyperuricemia Abnormality of the musculature Elevated erythrocyte sedimentation rate Chorioretinal atrophy Blurred vision Diabetes insipidus Epiphora Vitreous hemorrhage Cystoid macular edema Hypercalcemia Vitreous floaters 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 Abnormal conjunctiva morphology Abnormality of the cerebrospinal fluid Iridocyclitis Abnormal salivary gland morphology Anterior uveitis Dacryocystitis Chorioretinitis Abnormality of the adrenal glands Abnormality of the lymph nodes Skin plaque Generalized lymphadenopathy Erythema nodosum Pleural effusion Eosinophilia Tapered finger Abnormality of lipid metabolism Neonatal sepsis Intermittent thrombocytopenia Monocytosis Erythroid hypoplasia Congenital neutropenia Giant platelets Hypoplasia of the thymus Prominent superficial veins Varicose veins Premature loss of teeth Iron deficiency anemia Cataract Long fingers Unilateral renal agenesis Failure to thrive in infancy Tented upper lip vermilion Plagiocephaly Recurrent bacterial infections Broad thumb Mitral regurgitation Sparse scalp hair Renal agenesis Cor triatriatum Peripheral neuropathy Ventricular tachycardia Chest pain Osteolysis Decreased liver function Hyperpigmentation of the skin Anorexia Nephrolithiasis Subcutaneous nodule Palpitations Pancytopenia Syncope Sudden cardiac death Lymphadenopathy Skeletal muscle atrophy Erythema Facial palsy Arthritis Proximal muscle weakness Photophobia Glaucoma Arrhythmia Headache Renal insufficiency Blindness Cartilaginous ossification of larynx


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