Hypertension, and Pneumonia

Diseases related with Hypertension and Pneumonia

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

Top matches:

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

Karyomegalic interstitial nephritis is a rare, genetic renal disease characterized by slowly progressive, chronic, tubulointerstitial nephritis, leading to end-stage renal disease before the age of 50 years, manifesting with mild proteinuria, glucosuria and, occasionally, urinary sediment abnormalities (mainly hematuria). Mild extrarenal manifestations, such as recurrent upper respiratory tract infections and abnormal liver function tests, may be associated. Renal biopsy reveals severe, chronic, interstitial fibrosis and tubular changes, as well as hallmark karyomegalic tubular epithelial cells which line the proximal and distal tubules and have enlarged, hyperchromatic nuclei.

KARYOMEGALIC INTERSTITIAL NEPHRITIS Is also known as kin|systemic karyomegaly

Related symptoms:

  • Anemia
  • Hypertension
  • Renal insufficiency
  • Recurrent infections
  • Pneumonia


SOURCES: OMIM ORPHANET MENDELIAN

More info about KARYOMEGALIC INTERSTITIAL NEPHRITIS

Trimethylaminuria results from the abnormal presence of large amounts of volatile and malodorous trimethylamine within the body. This chemical, a tertiary aliphatic amine, is excreted in the urine, sweat (ichthyohidrosis), and breath, which take on the offensive odor of decaying fish (Mitchell, 1996).

TRIMETHYLAMINURIA; TMAU Is also known as fish-odor syndrome

Related symptoms:

  • Anemia
  • Hypertension
  • Splenomegaly
  • Depressivity
  • Hyperhidrosis


SOURCES: OMIM ORPHANET MENDELIAN

More info about TRIMETHYLAMINURIA; TMAU

Other less relevant 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

Related symptoms:

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


SOURCES: OMIM MENDELIAN

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

Medium match KAPOSI SARCOMA

Kaposi sarcoma (KS) is a rare human herpes virus 8 (HHV-8)-induced endothelial inflammatory neoplasm that develops is various clinically distinct settings, manifesting mostly as cutaneous lesions, or mucosal or visceral involvement.

KAPOSI SARCOMA Is also known as multiple idiopathic pigmented hemangiosarcoma, susceptibility to

Related symptoms:

  • Neoplasm
  • Hypertension
  • Fever
  • Fatigue
  • Edema


SOURCES: OMIM ORPHANET MENDELIAN

More info about KAPOSI SARCOMA

Monocytopenia with susceptibility to infections is a rare, genetic, primary immunodeficiency disorder characterized by profound circulating monocytopenia, B- and NK-cell lymphopenia and severe dentritic cell decrease, which manifests clinically with disseminated mycobacterial and viral infections, as well as opportunistic fungal and parasitic infections and frequent pulmonary alveolar proteinosis. Predisposition to developping myeloid neoplasms is associated.

MONOCYTOPENIA WITH SUSCEPTIBILITY TO INFECTIONS Is also known as dendritic cell, monocyte, b and nk lymphoid deficiency|dcml|dendritic cell, monocyte, b lymphocyte, and natural killer lymphocyte deficiency|monocytopenia with susceptibility to mycobacterial, fungal, and papillomavirus infections and myelodysplasia|monoc

Related symptoms:

  • Hearing impairment
  • Sensorineural hearing impairment
  • Anemia
  • Hypertension
  • Immunodeficiency


SOURCES: OMIM ORPHANET MENDELIAN

More info about MONOCYTOPENIA WITH SUSCEPTIBILITY TO INFECTIONS

Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia is an inborn error of folate metabolism due to deficiency of methylenetetrahydrofolate dehydrogenase-1. Manifestations may include hemolytic uremic syndrome, macrocytosis, epilepsy, hearing loss, retinopathy, mild mental retardation, lymphopenia involving all subsets, and low T-cell receptor excision circles. Folinic acid supplementation is an effective treatment (summary by Ramakrishnan et al., 2016).

COMBINED IMMUNODEFICIENCY AND MEGALOBLASTIC ANEMIA WITH OR WITHOUT HYPERHOMOCYSTEINEMIA; CIMAH Is also known as methylenetetrahydrofolate dehydrogenase 1 deficiency

Related symptoms:

  • Intellectual disability
  • Seizures
  • Hearing impairment
  • Sensorineural hearing impairment
  • Anemia


SOURCES: OMIM MENDELIAN

More info about COMBINED IMMUNODEFICIENCY AND MEGALOBLASTIC ANEMIA WITH OR WITHOUT HYPERHOMOCYSTEINEMIA; CIMAH

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

Generalized arterial calcification of infancy (GACI) is a severe autosomal recessive disorder characterized by calcification of the internal elastic lamina of muscular arteries and stenosis due to myointimal proliferation. GACI is often fatal within the first 6 months of life because of myocardial ischemia resulting in refractory heart failure (summary by Rutsch et al., 2003 and Cheng et al., 2005). Genetic Heterogeneity of Arterial CalcificationGeneralized arterial calcification of infancy-2 (GACI2 ) is caused by mutation in the ABCC6 gene (OMIM ) on chromosome 16p13.Homozygous or compound heterozygous mutation in the NT5E gene (OMIM ) can cause adult-onset of calcification of arteries and joints (OMIM ).

ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 1; GACI1 Is also known as iiac|idiopathic infantile arterial calcification|gaci|arteriopathy, occlusive infantile|arterial calcification, idiopathic infantile

Related symptoms:

  • Short stature
  • Hearing impairment
  • Failure to thrive
  • Hypertension
  • Respiratory distress


SOURCES: OMIM MENDELIAN

More info about ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 1; GACI1

Top 5 symptoms//phenotypes associated to Hypertension and Pneumonia

Symptoms // Phenotype % cases
Anemia Uncommon - Between 30% and 50% cases
Fever Uncommon - Between 30% and 50% cases
Respiratory distress Uncommon - Between 30% and 50% cases
Recurrent infections Uncommon - Between 30% and 50% cases
Immunodeficiency Uncommon - Between 30% and 50% cases

Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases

Vomiting Pulmonary arterial hypertension Hearing impairment Papule

Rare Symptoms - Less than 30% cases

Cyanosis Pain Respiratory failure Congestive heart failure Decreased antibody level in blood Neoplasm Recurrent pneumonia Abnormal lung morphology Diarrhea Pulmonary insufficiency Failure to thrive Edema Neutropenia Arthritis Seizures Lymphedema Leukopenia Lymphopenia Sensorineural hearing impairment Pancytopenia Rickets Short stature Respiratory tract infection Abnormality of the liver Carcinoma Premature loss of teeth Intellectual disability Severe viral infections Chronic myelomonocytic leukemia Monocytopenia Recurrent mycobacterium avium complex infections Abnormal natural killer cell morphology Arteriosclerosis Intellectual disability, mild Otosclerosis Acidosis Pallor Autoimmunity Retinopathy Metabolic acidosis Bilateral sensorineural hearing impairment Alveolar proteinosis Panniculitis Endocardial fibroelastosis Venous thrombosis Coronary artery calcification Generalized arterial calcification Arterial calcification Recurrent otitis media Vascular calcification Bone marrow hypocellularity Spontaneous abortion Coronary artery stenosis Myelodysplasia Recurrent fungal infections Myeloid leukemia Angioid streaks of the fundus Acute myeloid leukemia Severe sensorineural hearing impairment Aplastic anemia Recurrent viral infections Verrucae B lymphocytopenia Arterial stenosis Hypophosphatemic rickets Osteomalacia Conductive hearing impairment Headache Constipation Brachycephaly Proptosis Myocardial infarction Ventricular hypertrophy Genu valgum Arthralgia Premature loss of primary teeth Left ventricular hypertrophy Craniosynostosis Waddling gait Bone pain Increased intracranial pressure Chronic pain Hypercalcemia Chondrocalcinosis Papilledema Abnormality of the dentition Growth abnormality Ankylosis Anisocytosis Recurrent urinary tract infections Combined immunodeficiency Macrocytic anemia Thrombocytosis Severe combined immunodeficiency Antinuclear antibody positivity Pericardial effusion Megaloblastic anemia Hemolytic-uremic syndrome Glomerulosclerosis Folate deficiency Asthenia Septic arthritis Decreased methylcobalamin Thiamine-responsive megaloblastic anemia Hypophosphatemia Generalized hypotonia Feeding difficulties Nephrotic syndrome Lymphoproliferative disorder Otitis media Fish odor Depressivity Hyperhidrosis Anxiety Tachycardia Abnormal bleeding Abnormality of the cardiovascular system Alzheimer disease Body odor Trimethylaminuria Chronic tubulointerstitial nephritis Respiratory insufficiency Dyspnea Gastroesophageal reflux Scarring Cough Cirrhosis Bronchiectasis Scaling skin Clubbing Splenomegaly Mild proteinuria Increased antibody level in blood Stage 5 chronic kidney disease Jaundice Stroke Delayed puberty Heart murmur Renal insufficiency Elevated hepatic transaminase Proteinuria Abnormality of the kidney Hematuria Increased blood urea nitrogen Cholestasis Chronic kidney disease Nephritis Nephronophthisis Glycosuria Tubulointerstitial nephritis Elevated serum creatinine Tubular atrophy Normocytic anemia Pulmonary fibrosis Interstitial pulmonary abnormality Leukemia Abnormality of the gastrointestinal tract Lymphoma Gastrointestinal hemorrhage Neoplasm of the skin Hemangioma Sarcoma Hypermelanotic macule Abnormal retinal morphology Macule Abnormality of the lower limb Skin rash Abnormality of the spleen Cellular immunodeficiency Skin nodule Venous insufficiency Generalized lymphadenopathy Skin plaque Susceptibility to herpesvirus Neoplasm by anatomical site Hypothyroidism Lymphadenopathy Weight loss Exertional dyspnea Ground-glass opacification on pulmonary HRCT Polycythemia Pulmonary infiltrates Clubbing of fingers Right ventricular failure Crackles Alveolar cell carcinoma Hypocapnia Reticular pattern on pulmonary HRCT Honeycomb lung Postural instability Encephalopathy Dehydration Coarctation of aorta Epidermal acanthosis Long eyelashes Pustule Enlarged kidney Bronchiolitis Recurrent bronchiolitis Fatigue Periarticular calcification


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