Anemia, and Hypertension

Diseases related with Anemia and Hypertension

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


Top matches:

Low match SICKLE CELL-BETA-THALASSEMIA DISEASE SYNDROME


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

Low match ORTHOSTATIC HYPOTENSION 2; ORTHYP2


Orthostatic hypotension-2 is an autosomal recessive disorder characterized by severe orthostatic hypotension, recurrent hypoglycemia, and low norepinephrine levels. The disorder has onset in infancy or early childhood. Some patients may also have renal dysfunction and reduced life expectancy. The disorder results from a defect in the biosynthesis of norepinephrine from dopamine due to a cofactor deficiency.For a discussion of genetic heterogeneity of ORTHYP, see ORTHYP1 (OMIM ).

Related symptoms:

  • Anemia
  • Hypoglycemia
  • Vertigo
  • Tachycardia
  • Hypotension


SOURCES: OMIM MENDELIAN

More info about ORTHOSTATIC HYPOTENSION 2; ORTHYP2

Low match FAMILIAL PSEUDOHYPERKALEMIA


Familial pseudohyperkalemia (FP) is an inherited, mild, non-hemolytic subtype of hereditary stomatocytosis that is associated with a temperature-dependent anomaly in red cell membrane permeability to potassium that leads to high in vitro potassium levels in samples stored below 37°C. FP is not associated with additional hematological abnormalities, although affected individuals may show some mild abnormalities like macrocytosis.

Related symptoms:

  • Hypertension
  • Hyperkalemia
  • Reticulocytosis
  • Increased mean corpuscular volume
  • Stomatocytosis


SOURCES: ORPHANET MENDELIAN

More info about FAMILIAL PSEUDOHYPERKALEMIA

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Other less relevant matches:

Low match ATYPICAL HEMOLYTIC-UREMIC SYNDROME WITH B FACTOR ANOMALY


ATYPICAL HEMOLYTIC-UREMIC SYNDROME WITH B FACTOR ANOMALY Is also known as hemolytic-uremic syndrome without diarrhea with b factor anomaly|ahus, susceptibility to, 4|atypical hus with b factor anomaly|ahus with b factor anomaly|d-hus with b factor anomaly

Related symptoms:

  • Hypertension
  • Thrombocytopenia
  • Proteinuria
  • Hematuria
  • Acute kidney injury


SOURCES: ORPHANET OMIM MENDELIAN

More info about ATYPICAL HEMOLYTIC-UREMIC SYNDROME WITH B FACTOR ANOMALY

Low match ATYPICAL HEMOLYTIC-UREMIC SYNDROME WITH I FACTOR ANOMALY


ATYPICAL HEMOLYTIC-UREMIC SYNDROME WITH I FACTOR ANOMALY Is also known as atypical hus with i factor anomaly|d-hus with i factor anomaly|ahus, susceptibility to, 3|hemolytic-uremic syndrome without diarrhea with i factor anomaly|ahus with i factor anomaly

Related symptoms:

  • Anemia
  • Hypertension
  • Thrombocytopenia
  • Proteinuria
  • Hemolytic anemia


SOURCES: OMIM ORPHANET MENDELIAN

More info about ATYPICAL HEMOLYTIC-UREMIC SYNDROME WITH I FACTOR ANOMALY

Low match ATYPICAL HEMOLYTIC-UREMIC SYNDROME WITH THROMBOMODULIN ANOMALY


ATYPICAL HEMOLYTIC-UREMIC SYNDROME WITH THROMBOMODULIN ANOMALY Is also known as d-hus with thrombomodulin anomaly|ahus, susceptibility to, 6|atypical hus with thrombomodulin anomaly|ahus with thrombomodulin anomaly|hemolytic-uremic syndrome without diarrhea with thrombomodulin anomaly

Related symptoms:

  • Anemia
  • Hypertension
  • Renal insufficiency
  • Thrombocytopenia
  • Proteinuria


SOURCES: ORPHANET OMIM MENDELIAN

More info about ATYPICAL HEMOLYTIC-UREMIC SYNDROME WITH THROMBOMODULIN ANOMALY

Low match ATYPICAL HEMOLYTIC-UREMIC SYNDROME WITH C3 ANOMALY


ATYPICAL HEMOLYTIC-UREMIC SYNDROME WITH C3 ANOMALY Is also known as ahus with c3 anomaly|hemolytic-uremic syndrome without diarrhea with c3 anomaly|atypical hus with c3 anomaly|d-hus with c3 anomaly|ahus, susceptibility to, 5

Related symptoms:

  • Hypertension
  • Thrombocytopenia
  • Proteinuria
  • Stage 5 chronic kidney disease
  • Hematuria


SOURCES: ORPHANET OMIM MENDELIAN

More info about ATYPICAL HEMOLYTIC-UREMIC SYNDROME WITH C3 ANOMALY

Low match FOCAL SEGMENTAL GLOMERULOSCLEROSIS 3, SUSCEPTIBILITY TO; FSGS3


Focal segmental glomerulosclerosis (FSGS) is a pathologic entity associated clinically with proteinuria, the nephrotic syndrome (NPHS), and progressive loss of renal function. It is a common cause of end-stage renal disease (ESRD) (Meyrier, 2005).For a general phenotypic description and a discussion of genetic heterogeneity of focal segmental glomerulosclerosis and nephrotic syndrome, see FSGS1 (OMIM ).

FOCAL SEGMENTAL GLOMERULOSCLEROSIS 3, SUSCEPTIBILITY TO; FSGS3 Is also known as glomerulosclerosis, focal segmental, 3, susceptibility to

Related symptoms:

  • Failure to thrive
  • Anemia
  • Hypertension
  • Renal insufficiency
  • Proteinuria


SOURCES: OMIM MENDELIAN

More info about FOCAL SEGMENTAL GLOMERULOSCLEROSIS 3, SUSCEPTIBILITY TO; FSGS3

Low match IMMUNOGLOBULIN-MEDIATED MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS


Nephrotic syndrome type 7 is an autosomal recessive renal disease characterized by onset of nephrotic syndrome with proteinuria usually in the first decade of life. The disorder is progressive, and some patients develop end-stage renal disease within several years. Renal biopsy typically shows membranoproliferative glomerulonephritis. Some patients may benefit from immunosuppressive therapy (summary by Ozaltin et al., 2013).Atypical hemolytic uremic syndrome-7 is characterized by acute onset in the first year of life of microangiopathic hemolytic anemia, thrombocytopenia, and renal failure. After the acute episode, most patients develop chronic renal insufficiency. Unlike other genetic forms of aHUS, AHUS7 is not related to abnormal activation of the complement system (summary by Lemaire et al., 2013).For a general phenotypic description and a discussion of genetic heterogeneity of nephrotic syndrome, see NPHS1 (OMIM ).For a general phenotypic description and a discussion of genetic heterogeneity of aHUS, see AHUS1 (OMIM ).

IMMUNOGLOBULIN-MEDIATED MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS Is also known as ig-mediated mpgn|immunoglobulin-mediated mpgn|ig-mediated membranoproliferative glomerulonephritis|nephrotic syndrome, type 7, with membranoproliferative glomerulonephritis

Related symptoms:

  • Anemia
  • Hypertension
  • Renal insufficiency
  • Thrombocytopenia
  • Proteinuria


SOURCES: ORPHANET OMIM MENDELIAN

More info about IMMUNOGLOBULIN-MEDIATED MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS

Low match BILE ACID SYNTHESIS DEFECT, CONGENITAL, 5; CBAS5


Related symptoms:

  • Anemia
  • Hypertension
  • Hepatomegaly
  • Splenomegaly
  • Jaundice


SOURCES: OMIM MENDELIAN

More info about BILE ACID SYNTHESIS DEFECT, CONGENITAL, 5; CBAS5

Top 5 symptoms//phenotypes associated to Anemia and Hypertension

Symptoms // Phenotype % cases
Proteinuria Common - Between 50% and 80% cases
Thrombocytopenia Uncommon - Between 30% and 50% cases
Microangiopathic hemolytic anemia Uncommon - Between 30% and 50% cases
Hemolytic-uremic syndrome Uncommon - Between 30% and 50% cases
Acute kidney injury Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases


Hematuria Anuria Increased blood urea nitrogen Elevated serum creatinine Stage 5 chronic kidney disease Renal insufficiency Hemolytic anemia

Rare Symptoms - Less than 30% cases


Nephrotic syndrome Microscopic hematuria Focal segmental glomerulosclerosis Glomerulosclerosis Jaundice Abnormality of the liver Abnormality of the coagulation cascade Portal hypertension Hepatic fibrosis Pancytopenia Hepatic failure Elevated hepatic transaminase Meningitis Hepatosplenomegaly Splenomegaly Hepatomegaly Thickening of the glomerular basement membrane Membranoproliferative glomerulonephritis Glomerulopathy Glomerulonephritis Pain Chronic kidney disease Tachycardia Pneumonia Stroke Delayed puberty Heart murmur Hypoglycemia Vertigo Hypotension Failure to thrive Orthostatic hypotension Recurrent hypoglycemia Hyperkalemia Reticulocytosis Increased mean corpuscular volume Stomatocytosis Episodic hemolytic anemia Iron deficiency anemia



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