Hypertension, and Sinusitis

Diseases related with Hypertension and Sinusitis

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

Top matches:

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

Severe combined immunodeficiency (SCID) due to adenosine deaminase (ADA) deficiency is a form of SCID characterized by profound lymphopenia and very low immunoglobulin levels of all isotypes resulting in severe and recurrent opportunistic infections.

SEVERE COMBINED IMMUNODEFICIENCY DUE TO ADENOSINE DEAMINASE DEFICIENCY Is also known as ada deficiency|ada-scid|scid due to adenosine deaminase deficiency|scid due to ada deficiency|scid due to ada deficiency, early-onset

Related symptoms:

  • Global developmental delay
  • Failure to thrive
  • Hypertension
  • Hepatomegaly
  • Abnormality of the skeletal system


SOURCES: MESH ORPHANET OMIM MENDELIAN

More info about SEVERE COMBINED IMMUNODEFICIENCY DUE TO ADENOSINE DEAMINASE DEFICIENCY

Resistance to thyroid-stimulating hormone (TSH; see {188540}), a hallmark of congenital nongoitrous hypothyroidism, causes increased levels of plasma TSH and low levels of thyroid hormone. Only a subset of patients develop frank hypothyroidism; the remainder are euthyroid and asymptomatic (so-called compensated hypothyroidism) and are usually detected by neonatal screening programs (Paschke and Ludgate, 1997). Genetic Heterogeneity of Congenital Nongoitrous HypothyroidismCHNG2 (OMIM ) is caused by mutation in the PAX8 gene (OMIM ) on chromosome 2q12-q14; CHNG3 (OMIM ) maps to a locus on chromosome 15q25.3; CHNG4 (OMIM ) is caused by mutation in the TSHB gene (OMIM ) on chromosome 1p13; CHNG5 (OMIM ) is caused by mutation in the NKX2-5 gene (OMIM ) on chromosome 5q34; and CHNG6 (OMIM ) is caused by mutation in the THRA gene (OMIM ) on chromosome 17q21.1.

HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 1; CHNG1 Is also known as tsh resistance|hypothyroidism, congenital, due to tsh resistance|hypothyroidism, nonautoimmune|rtsh|thyrotropin resistance|hypothyroidism due to unresponsiveness to thyrotropin|thyroid-stimulating hormone, resistance to

Related symptoms:

  • Intellectual disability
  • Global developmental delay
  • Short stature
  • Hearing impairment
  • Muscular hypotonia


SOURCES: OMIM ORPHANET MENDELIAN

More info about HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 1; CHNG1

Other less relevant matches:

Medium 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

Granulomatosis with polyangiitis is a small-vessel necrotizing vasculitis characterised by the association of inflammation of the vessel wall and peri- and extravascular granulomatosis.

GRANULOMATOSIS WITH POLYANGIITIS Is also known as wegener granulomatosis, formerly|gpa|wg, formerly

Related symptoms:

  • Seizures
  • Hearing impairment
  • Sensorineural hearing impairment
  • Pain
  • Visual impairment


SOURCES: ORPHANET OMIM MESH MENDELIAN

More info about GRANULOMATOSIS WITH POLYANGIITIS

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

Autoimmune polyendocrinopathy type 1, or APECED syndrome, is a genetic disease that manifests in childhood or early adolescence with a combination of chronic mucocutaneous candidiasis, hypoparathyroidism and autoimmune adrenal failure.

AUTOIMMUNE POLYENDOCRINOPATHY TYPE 1 Is also known as autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy|apeced|autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome|autoimmune hypoparathyroidism-chronic candidiasis-addison disease syndrome|apeced syndrome|polyglandular autoimmu

Related symptoms:

  • Seizures
  • Abnormal facial shape
  • Cataract
  • Anemia
  • Visual impairment


SOURCES: OMIM ORPHANET MENDELIAN

More info about AUTOIMMUNE POLYENDOCRINOPATHY TYPE 1

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 ACROOSTEOLYSIS

Related symptoms:

  • Short stature
  • Hearing impairment
  • Scoliosis
  • Hypertelorism
  • Failure to thrive


SOURCES: OMIM MESH MENDELIAN

More info about ACROOSTEOLYSIS

SICKLE CELL-BETA-THALASSEMIA DISEASE SYNDROME Is also known as hbs-beta-thalassemia syndrome

Related symptoms:

  • Pain
  • Anemia
  • Hypertension
  • Pneumonia
  • Jaundice


SOURCES: ORPHANET MENDELIAN

More info about SICKLE CELL-BETA-THALASSEMIA DISEASE SYNDROME

Top 5 symptoms//phenotypes associated to Hypertension and Sinusitis

Symptoms // Phenotype % cases
Recurrent respiratory infections Common - Between 50% and 80% cases
Failure to thrive Uncommon - Between 30% and 50% cases
Pain Uncommon - Between 30% and 50% cases
Global developmental delay Uncommon - Between 30% and 50% cases
Hearing impairment Uncommon - Between 30% and 50% cases

Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases

Respiratory tract infection Recurrent otitis media Asthma Seizures Alopecia Chronic obstructive pulmonary disease Delayed puberty Otitis media Recurrent pneumonia Short stature Cataract Hepatomegaly Splenomegaly Pancreatitis Hypotension Intestinal obstruction Emphysema Peripheral neuropathy Pulmonary fibrosis Autoimmune thrombocytopenia Retinopathy Pneumonia Visual impairment Autoimmunity Diabetes insipidus Hypotrichosis Recurrent bronchitis Intellectual disability Hepatitis Chronic diarrhea Dry skin Paresthesia Nausea Respiratory distress Vomiting Diarrhea Dilatation Recurrent infections Diabetes mellitus Abdominal pain Respiratory failure Optic atrophy Abnormality of the liver Jaundice Infertility Cough Constipation Hypogonadism Hypothyroidism Decreased antibody level in blood Abdominal distention Fatigue

Rare Symptoms - Less than 30% cases

Abnormal facial shape Hydronephrosis Umbilical hernia Sleep disturbance Coarse facial features Goiter Growth abnormality Sensorineural hearing impairment Osteoporosis Chronic sinusitis Recurrent sinusitis Pulmonic stenosis Ventricular septal defect Feeding difficulties Malar flattening Pulmonary arterial hypertension Cerebral calcification Arrhythmia Depressivity Wide nose Short distal phalanx of finger Abnormality of the thyroid gland Growth delay Respiratory insufficiency Female hypogonadism Anemia Rod-cone dystrophy Photophobia Pallor Pigmentary retinopathy Hypergonadotropic hypogonadism Abnormality of the fingernails Cholelithiasis Constriction of peripheral visual field Chronic active hepatitis Thyroiditis Scoliosis Short neck Abnormality of the dentition Kyphosis Patent ductus arteriosus Abnormality of the kidney Thickened skin Short toe Generalized hirsutism Vitiligo Absence seizures Cardiomyopathy Stroke Renal insufficiency Headache Visual loss Weight loss Dyspnea Arthralgia Myalgia Proteinuria Skin rash Nausea and vomiting Growth hormone deficiency Hematuria Gastrointestinal hemorrhage Diplopia Skin ulcer Glomerulonephritis Chronic otitis media Glomerulopathy Pericarditis Elevated C-reactive protein level Nephropathy Alopecia totalis Cirrhosis Malnutrition Elevated hepatic transaminase Insulin resistance Nephrocalcinosis Tachypnea Gastroesophageal reflux Portal hypertension Immunodeficiency Purpura Dehydration Bronchitis Wheezing Hemoptysis Sepsis Hepatosplenomegaly Allergy Obstructive lung disease Chronic infection Bronchiectasis Recurrent upper respiratory tract infections Malabsorption Severe B lymphocytopenia Carcinoma Scarring Carious teeth Polyphagia Hypoventilation Severe sensorineural hearing impairment Thoracic scoliosis Subcapsular cataract Increased number of teeth Hyperuricemia Glycosuria Progressive sensorineural hearing impairment Agenesis of permanent teeth Short finger Pes planus Chorioretinal atrophy Pericardial effusion Retinal atrophy Abnormal retinal morphology Truncal obesity Urinary urgency Hydroureter Polyuria Glucose intolerance Hyperglycemia Deeply set eye Hyperostosis Acne Insulin-resistant diabetes mellitus Alopecia of scalp Peripheral visual field loss Tubular atrophy Decreased HDL cholesterol concentration Ovarian cyst High-frequency hearing impairment Restrictive cardiomyopathy Autism Esophageal varix Chronic fatigue Myocardial fibrosis Male hypogonadism Oligospermia Kyphoscoliosis Myocarditis Acute hepatic failure Conductive hearing impairment Elevated serum creatinine Right ventricular hypertrophy Attenuation of retinal blood vessels Tubulointerstitial nephritis Pendular nystagmus Gingivitis Ketoacidosis Broad foot Posterior subcapsular cataract Oligomenorrhea Poor coordination Hyperventilation Impaired vibratory sensation Aplasia/Hypoplasia of the cerebellum Retinal degeneration Progressive visual loss Anorexia Hypermetropia Left ventricular hypertrophy Recurrent urinary tract infections Involuntary movements Hypertriglyceridemia Epidermal acanthosis Type II diabetes mellitus Cardiomegaly Optic disc pallor Cyanosis Specific learning disability Decreased testicular size Dilated cardiomyopathy Round face Urinary incontinence Vesicoureteral reflux Ascites Hepatic steatosis Retinal dystrophy Ophthalmoplegia Hirsutism Hepatic failure Tachycardia Stage 5 chronic kidney disease Lymphadenopathy Generalized tonic-clonic seizures Abnormality of retinal pigmentation Obsessive-compulsive behavior Atherosclerosis Nephritis Polydipsia Lipodystrophy Hyperinsulinemia Precocious puberty Elevated alkaline phosphatase Abnormality of the hand Polycystic ovaries Abnormal renal morphology Cone/cone-rod dystrophy Hypercholesterolemia Hyperlipidemia Acanthosis nigricans Decreased liver function Macular degeneration Irritability Accelerated skeletal maturation Hypogonadotrophic hypogonadism Postnatal growth retardation Autistic behavior Increased body weight Horizontal nystagmus Sparse hair Nyctalopia Gynecomastia Hyperpigmentation of the skin Hepatic fibrosis Menstrual irregularities Abnormal renal physiology Endocardial fibroelastosis Osteopenia Full cheeks Recurrent fractures Downturned corners of mouth Iris coloboma Thick eyebrow Thin vermilion border Joint hypermobility Joint hyperflexibility Synophrys Dolichocephaly Pectus carinatum Telecanthus Joint laxity Skeletal dysplasia Narrow mouth Dental malocclusion Inguinal hernia Hypospadias Hernia Long philtrum Hydrocephalus Anteverted nares Downslanted palpebral fissures Macrocephaly Myopia Wide nasal bridge Brachydactyly Low-set ears Cleft palate Micrognathia Intestinal malrotation Bowing of the long bones Abnormality of the femoral head Osteolytic defects of the phalanges of the hand Osteolytic defects of the phalanges of the toes Partial absence of toe Hypoplastic 5th lumbar vertebrae Basilar invagination Premature loss of permanent teeth Basilar impression Flank pain Absent frontal sinuses Rough bone trabeculation Biconcave vertebral bodies Respiratory arrest Platybasia Decreased skull ossification Mitral stenosis Periodontitis Bone pain Multiple renal cysts Patellar dislocation Syringomyelia Prominent occiput Delayed cranial suture closure Open bite Abnormality of the voice Polycystic kidney dysplasia Coarse hair Arnold-Chiari malformation Osteolysis Wormian bones Low anterior hairline Aortic valve stenosis Hypertelorism Vitreous haze Retinal pigment epithelial atrophy Multinodular goiter Epigastric pain Abnormality of dental color Lumbar scoliosis Abnormality of the urethra Abnormal spermatogenesis Decreased glomerular filtration rate Abnormality of the optic disc First degree atrioventricular block Melena Hematemesis Frontal balding Increased total bilirubin Vertical nystagmus Bull's eye maculopathy Abnormality of female external genitalia Urethral stricture Hepatic encephalopathy Urethral stenosis Achromatopsia Acute pancreatitis Chills Pyelonephritis Poor fine motor coordination Urinary retention Arteriosclerosis Tubulointerstitial fibrosis Testicular atrophy Abnormal left ventricle morphology Polydactyly Disinhibition Abnormal chorioretinal morphology Impaired temperature sensation Localized hirsutism Abnormal adipose tissue morphology Abnormality of renal calyx morphology Abnormality of prothrombin EEG with occipital slowing Precocious puberty in females Abnormal retinal artery morphology Widely-spaced incisors Recurrent cystitis Glue ear Unilateral breast hypoplasia Dilatation of the bladder Thickened ears Granular macular appearance Receptive language delay Hyperostosis frontalis interna Nonproductive cough Abnormal muscle tone Hepatic necrosis Albuminuria Renovascular hypertension Squared iliac bones Urethral obstruction Abnormality of the pituitary gland Hypoplastic male external genitalia Chronic hepatic failure Exudative retinopathy Facial hirsutism ST segment depression Multifocal atrial tachycardia Childhood-onset truncal obesity High-frequency sensorineural hearing impairment Increased circulating androgen level Hyperkeratosis Absent specific antibody response Hyperhidrosis Spontaneous abortion Neutropenia Short hallux Pulmonary artery stenosis Irregular vertebral endplates Epiphyseal stippling Inflammatory abnormality of the skin Mixed hearing impairment Aortic aneurysm Nasal speech Dermal atrophy Deep philtrum Progressive hearing impairment Cutis laxa Leukodystrophy Peripheral pulmonary artery stenosis Short thumb Short phalanx of finger Lymphopenia Sloping forehead Recurrent bacterial infections Memory impairment Underdeveloped nasal alae Leukoencephalopathy Eosinophilia Long face Abnormality of pelvic girdle bone morphology Combined immunodeficiency Macrotia Thyroid carcinoma Shortening of all distal phalanges of the fingers IgA deficiency Microscopic nephrocalcinosis Paralysis Productive cough Arthritis Pancreatic adenocarcinoma Meconium ileus Recurrent bronchopulmonary infections Proptosis Obstructive azoospermia Absent vas deferens Elevated sweat chloride Biliary tract obstruction Cellular metachromasia Echogenic fetal bowel Fever Short nail Abnormality of the skeletal system Platyspondyly Cartilaginous ossification of larynx Premature fusion of phalangeal epiphyses Cartilaginous ossification of nose Calcification of the auricular cartilage Costal cartilage calcification Soft, doughy skin Tracheal atresia Calcification of cartilage Arterial calcification Pulmonary artery hypoplasia Abdominal aortic aneurysm Papillary thyroid carcinoma Autoimmune hemolytic anemia Midface retrusion Chronic pancreatitis Anxiety Abnormality of epiphysis morphology Nephrolithiasis Large fontanelles Abnormality of the face Depressed nasal ridge Increased IgE level Macroglossia Pulmonary insufficiency Oral cleft Decrease in T cell count B lymphocytopenia Feeding difficulties in infancy Abnormality of the eye Diffuse mesangial sclerosis Reduced tendon reflexes Recurrent fungal infections Anterior rib cupping Aplasia of the thymus Cortical sclerosis Recurrent opportunistic infections Immunoglobulin IgG2 deficiency Absence of lymph node germinal center Intellectual disability, severe Absent tonsils Abnormality of humoral immunity Muscular hypotonia Lack of T cell function Anti-thyroid peroxidase antibody positivity Abnormality of the hair Oligodontia Severe combined immunodeficiency Hoarse cry Intellectual disability, mild Recurrent lower respiratory tract infections Depressed nasal bridge B-cell lymphoma Recurrent viral infections Abnormality of reproductive system physiology Large posterior fontanelle Thyroid dysgenesis Compensated hypothyroidism Angiokeratoma corporis diffusum Thyroid agenesis Abnormal pericardium morphology Ectopic thyroid Increased thyroid-stimulating hormone level Anosmia Thyroid hypoplasia Primary hypothyroidism Pseudohypoparathyroidism Anterior hypopituitarism Hypothermia Abnormal eyelid morphology Palpebral edema Congenital hypothyroidism Prolonged neonatal jaundice Verrucae Tracheoesophageal fistula IgM deficiency Abnormality of vision Cellular immunodeficiency Secretory diarrhea Papule Myoclonus Hypocalcemia Asplenia Antinuclear antibody positivity Adrenal hyperplasia Increased circulating cortisol level Hypoparathyroidism Primary adrenal insufficiency Metaphyseal dysplasia Macular atrophy Adrenal insufficiency Hypopigmented skin patches Opacification of the corneal stroma Azoospermia Type I diabetes mellitus Hypoplasia of dental enamel Abnormality of the cerebral vasculature Hypercalciuria Muscle cramps Rigidity Clubbing Reduced visual acuity Steatorrhea Abnormality of the periungual region Abnormal size of pituitary gland Decreased circulating androgen level Abnormal lymphocyte morphology Severe viral infections Decreased serum insulin-like growth factor 1 Adrenocorticotropin deficient adrenal insufficiency Chronic mucocutaneous candidiasis Achalasia Decreased circulating ACTH level Strabismus Hyporeflexia Clinodactyly Encephalopathy Obesity Dystonia Behavioral abnormality Reduced red cell adenosine deaminase activity Congestive heart failure Blindness Dyskinesia Motor delay Delayed speech and language development Cognitive impairment Nystagmus Tetany Ataxia Patchy atrophy of the retinal pigment epithelium Decreased circulating parathyroid hormone level Salt craving Abnormal lung morphology Chronic atrophic gastritis Abnormality of calcium-phosphate metabolism Chronic hepatitis Alopecia areata Keratoconjunctivitis Gastritis Central diabetes insipidus Alopecia universalis Decreased circulating aldosterone level Hypoglycemic coma Recurrent pharyngitis Nasal polyposis Hemiplegia Tracheal stenosis Myositis Gangrene Pulmonary infiltrates Neoplasm of the pancreas Chronic lung disease Elevated erythrocyte sedimentation rate Petechiae Restrictive ventilatory defect Cor pulmonale Stridor Abnormality of the pancreas Pleural effusion Venous thrombosis Concave nasal ridge Cranial nerve paralysis Conjunctivitis Vasculitis Meningitis Hoarse voice Biliary cirrhosis Ileus Subcutaneous nodule Myocardial infarction Epistaxis Pneumothorax Chest pain Sensory neuropathy Rectal prolapse Angina pectoris Cerebral ischemia Neoplasm Episcleritis Autoimmune antibody positivity Decreased circulating cortisol level Recurrent hypoglycemia Male infertility Hyperkalemia Hyponatremia Psoriasiform dermatitis Nail dystrophy Prostatitis Recurrent intrapulmonary hemorrhage Scleritis Increased inflammatory response Arteritis Abnormal oral cavity morphology Abnormality of the nose Ureteral stenosis Endocarditis Neuritis Granulomatosis Pleuritis Subglottic stenosis Ocular pain Rhinorrhea Periorbital edema Exocrine pancreatic insufficiency Inflammatory abnormality of the eye Nasal obstruction Recurrent corneal erosions Abnormality of the hypothalamus-pituitary axis Heart murmur


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