Hypertension, and Abnormality of the skin

Diseases related with Hypertension and Abnormality of the skin

In the following list you will find some of the most common rare diseases related to Hypertension and Abnormality of the skin 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

Liddle syndrome, or pseudoaldosteronism, is an autosomal dominant form of salt-sensitive hypertension characterized by suppressed plasma renin and aldosterone, hypokalemia, and metabolic alkalosis (summary by Salih et al., 2017).For a discussion of genetic heterogeneity of Liddle syndrome, see {177200}.

Related symptoms:

  • Hypertension
  • Hypokalemia
  • Alkalosis
  • Metabolic alkalosis


SOURCES: OMIM MENDELIAN

More info about LIDDLE SYNDROME 3; LIDLS3

AORTIC VALVE DISEASE 2; AOVD2 Is also known as bicuspid aortic valve|aortic valve stenosis

Related symptoms:

  • Hypertension
  • Coarctation of aorta
  • Aortic valve stenosis
  • Bicuspid aortic valve
  • Heart murmur


SOURCES: OMIM MENDELIAN

More info about AORTIC VALVE DISEASE 2; AOVD2

Other less relevant matches:

Related symptoms:

  • Neoplasm
  • Hypertension
  • Hyperhidrosis
  • Vertigo
  • Tachycardia


SOURCES: OMIM MENDELIAN

More info about PARAGANGLIOMAS 5; PGL5

HEMORRHAGE, INTRACEREBRAL, SUSCEPTIBILITY TO; ICH Is also known as stroke, hemorrhagic, susceptibility to

Related symptoms:

  • Seizures
  • Hypertension
  • Stroke
  • Lower limb muscle weakness
  • Type II diabetes mellitus


SOURCES: OMIM MESH MENDELIAN

More info about HEMORRHAGE, INTRACEREBRAL, SUSCEPTIBILITY TO; ICH

Approximately 40 million people take ACE inhibitors (ACEi) to treat hypertension and cardiovascular disease. A small proportion of white patients who take ACEi (0.1-0.7%) develop angioedema (AEACEI) (Israili and Hall, 1992; Vleeming et al., 1998), a potentially life-threatening side effect characterized by swelling of the face, lips, tongue, and airway that can lead to suffocation and death if severe. ACEi-associated angioedema is 4 to 5 times more prevalent among African Americans (Brown et al., 1996; Coats, 2002). Other risk factors include female sex, smoking, immunosuppressant therapy, and seasonal allergies. The pathophysiology of ACEi-associated angioedema is thought to be related to increased circulating bradykinin, which is normally degraded by ACE. During pharmacologic ACE inhibition, bradykinin is primarily degraded by aminopeptidase P (summary by Duan et al., 2005 and Woodard-Grice et al., 2010). Aminopeptidase P is encoded by 3 genes: XPNPEP1 (OMIM ) on chromosome 10q25, XPNPEP2 (OMIM ) on chromosome Xq25, and XPNPEP3 (OMIM ) on chromosome 22q13.

Related symptoms:

  • Hypertension
  • Abnormality of the cardiovascular system
  • Angioedema


SOURCES: OMIM MESH MENDELIAN

More info about ANGIOEDEMA INDUCED BY ACE INHIBITORS, SUSCEPTIBILITY TO; AEACEI

Related symptoms:

  • Elevated diastolic blood pressure


SOURCES: OMIM MENDELIAN

More info about HYPERTENSION, DIASTOLIC, RESISTANCE TO

Hereditary North American Indian childhood cirrhosis is a severe autosomal recessive intrahepatic cholestasis that has only been described in aboriginal children from northwestern Quebec. Manifesting first as transient neonatal jaundice, the disease evolves into periportal fibrosis and cirrhosis during a period ranging from childhood to adolescence.

Related symptoms:

  • Jaundice
  • Cirrhosis
  • Cholestasis
  • Portal hypertension
  • Prolonged neonatal jaundice


SOURCES: MESH ORPHANET OMIM MENDELIAN

More info about HEREDITARY NORTH AMERICAN INDIAN CHILDHOOD CIRRHOSIS

Dyslexia is a disorder manifested by difficulty learning to read despite conventional instruction, adequate intelligence, and sociocultural opportunity. It is among the most common neurodevelopmental disorders, with a prevalence of 5 to 12%. Although there is evidence for familial clustering and heritability, the disorder is considered a complex multifactorial trait (Schumacher et al., 2007). Genetic Heterogeneity of Susceptibility to DyslexiaAdditional dyslexia susceptibility loci include DYX2 (OMIM ) on chromosome 6p22, DYX3 (OMIM ) on chromosome 2p16-p15, DYX5 (OMIM ) on chromosome 3p12-q13, DYX6 (OMIM ) on chromosome 18p11.2, DYX8 (OMIM ) on chromosome 1p36-p34, and DYX9 (OMIM ) on chromosome Xq27.3.See MAPPING for other possible dyslexia susceptibility loci, including DYX4 and DYX7.

DYSLEXIA, SUSCEPTIBILITY TO, 1; DYX1 Is also known as word-blindness, congenital|reading disability, specific, 1

Related symptoms:

  • Hypertension
  • Neurological speech impairment
  • Dyslexia


SOURCES: OMIM MENDELIAN

More info about DYSLEXIA, SUSCEPTIBILITY TO, 1; DYX1

Related symptoms:

  • Neoplasm
  • Hypertension
  • Abnormality of metabolism/homeostasis
  • Depressivity
  • Hypotension


SOURCES: MESH OMIM MENDELIAN

More info about DRUG METABOLISM, POOR, CYP2D6-RELATED

Top 5 symptoms//phenotypes associated to Hypertension and Abnormality of the skin

Symptoms // Phenotype % cases
Jaundice Rare - less than 30% cases
Stroke Rare - less than 30% cases
Heart murmur Rare - less than 30% cases
Neoplasm Rare - less than 30% cases
Pain Rare - less than 30% cases

Other less frequent symptoms

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

Rare Symptoms - Less than 30% cases

Portal hypertension Abnormality of the cardiovascular system Angioedema Elevated diastolic blood pressure Cirrhosis Cholestasis Neurological speech impairment Prolonged neonatal jaundice Biliary cirrhosis Type II diabetes mellitus Dyslexia Abnormality of metabolism/homeostasis Depressivity Hypotension Cerebral hemorrhage Pheochromocytoma Lower limb muscle weakness Aortic valve stenosis Pneumonia Delayed puberty Hypokalemia Alkalosis Metabolic alkalosis Coarctation of aorta Bicuspid aortic valve Seizures Calcification of the aorta Hyperhidrosis Vertigo Tachycardia Anemia Paraganglioma Schizophrenia


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