Lymphoma, and Ischemic stroke

Diseases related with Lymphoma and Ischemic stroke

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


Top matches:

Medium match ESSENTIAL THROMBOCYTHEMIA


Essential thrombocythemia (ET) is a myeloproliferative neoplasm (MPN, see this term) characterized by a sustained elevation of platelet number (> 450 x 109/L) with a tendency for thrombosis and hemorrhage.

ESSENTIAL THROMBOCYTHEMIA Is also known as thrombocytosis 1|essential thrombocytosis|et

Related symptoms:

  • Pain
  • Hypertension
  • Hepatomegaly
  • Abnormality of the skeletal system
  • Respiratory distress


SOURCES: ORPHANET OMIM MENDELIAN

More info about ESSENTIAL THROMBOCYTHEMIA

Medium match SCHIMKE IMMUNO-OSSEOUS DYSPLASIA


Schimke immuno-osseous dysplasia (SIOD) is a multisystem disorder characterized by spondyloepiphyseal dysplasia and disproportionate short stature, facial dysmorphism, T-cell immunodeficiency, and glomerulonephritis with nephrotic syndrome.

SCHIMKE IMMUNO-OSSEOUS DYSPLASIA Is also known as immunoosseous dysplasia, schimke type|schimke syndrome|spondyloepiphyseal dysplasia-nephrotic syndrome

Related symptoms:

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


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about SCHIMKE IMMUNO-OSSEOUS DYSPLASIA

Medium match WALDENSTRÖM MACROGLOBULINEMIA


Waldenström macroglobulinemia (WM) is an indolent B-cell lymphoproliferative disorder characterized by the accumulation of monoclonal cells in the bone marrow and peripheral lymphoid tissues, and associated with the production of serum immunoglobulin M (IgM) monoclonal protein.

Related symptoms:

  • Hearing impairment
  • Ataxia
  • Neoplasm
  • Anemia
  • Peripheral neuropathy


SOURCES: OMIM ORPHANET MENDELIAN

More info about WALDENSTRÖM MACROGLOBULINEMIA

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Other less relevant matches:

Medium match CUTIS MARMORATA TELANGIECTATICA CONGENITA


Cutis marmorata telangiectatica congenita (CMTC) is a congenital localized or generalized vascular anomaly characterized by a persistent cutis marmorata pattern with a marbled bluish to deep purple appearance, spider nevus-like telangiectasia, phlebectasia and, occasionally, ulceration and atrophy of the affected skin.

CUTIS MARMORATA TELANGIECTATICA CONGENITA Is also known as megalencephaly-cutis marmorata telangiectatica congenita|cmtc|mcmtc|megalencephaly-capillary malformation syndrome|macrocephaly-cutis marmorata telangiectatica congenita|mcm|macrocephaly-capillary malformation

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Generalized hypotonia
  • Scoliosis


SOURCES: OMIM ORPHANET MENDELIAN

More info about CUTIS MARMORATA TELANGIECTATICA CONGENITA

Low match PAROXYSMAL NOCTURNAL HEMOGLOBINURIA


Paroxysmal nocturnal hemoglobinuria (PNH) is an acquired clonal hematopoietic stem cell disorder characterized by corpuscular hemolytic anemia, bone marrow failure and frequent thrombotic events.

PAROXYSMAL NOCTURNAL HEMOGLOBINURIA Is also known as marchiafava-micheli disease|pnh

Related symptoms:

  • Muscle weakness
  • Fatigue
  • Dysphagia
  • Abdominal pain
  • Pallor


SOURCES: ORPHANET OMIM MENDELIAN

More info about PAROXYSMAL NOCTURNAL HEMOGLOBINURIA

Low match FAMILIAL THROMBOCYTOSIS


Familial thrombocytosis is a type of thrombocytosis, a sustained elevation of platelet numbers, which affects the platelet/megakaryocyte lineage and may create a tendency for thrombosis and hemorrhage but does not cause myeloproliferation.

FAMILIAL THROMBOCYTOSIS Is also known as familial thrombocythemia|hereditary thrombocythemia

Related symptoms:

  • Seizures
  • Dysarthria
  • Splenomegaly
  • Headache
  • Hyperhidrosis


SOURCES: ORPHANET MENDELIAN

More info about FAMILIAL THROMBOCYTOSIS

Low match POLYCYTHEMIA VERA


Polycythemia vera (PV) is an acquired myeloproliferative disorder characterized by an elevated absolute red blood cell mass caused by uncontrolled red blood cell production, frequently associated with uncontrolled white blood cell and platelet production.

POLYCYTHEMIA VERA Is also known as polycythemia rubra vera|acquired primary erythrocytosis|prv|vaquez disease|osler-vaquez disease|pv

Related symptoms:

  • Neoplasm
  • Visual impairment
  • Hypertension
  • Hepatomegaly
  • Fatigue


SOURCES: ORPHANET MESH OMIM MENDELIAN

More info about POLYCYTHEMIA VERA

Low match PRIMARY FAMILIAL POLYCYTHEMIA


Primary familial polycythemia is an inherited hematological disorder resulting from mutations in the erythropoietin (EPO) receptor and is characterized by an elevated absolute red blood cell mass caused by uncontrolled red blood cell production in the presence of low EPO levels.

PRIMARY FAMILIAL POLYCYTHEMIA Is also known as polycythemia, primary familial and congenital|primary familial and congenital polycythemia|familial erythrocytosis|erythrocytosis, autosomal dominant benign|pfcp|congenital polycythemia due to erythropoietin receptor mutation|congenital erythrocytosis due

Related symptoms:

  • Pain
  • Hypertension
  • Fatigue
  • Respiratory distress
  • Splenomegaly


SOURCES: OMIM ORPHANET MENDELIAN

More info about PRIMARY FAMILIAL POLYCYTHEMIA

Low match SICKLE CELL ANEMIA


Sickle cell anemias are chronic hemolytic diseases that may induce three types of acute accidents: severe anemia, severe bacterial infections, and ischemic vasoocclusive accidents (VOA) caused by sickle-shaped red blood cells obstructing small blood vessels and capillaries. Many diverse complications can occur.

SICKLE CELL ANEMIA Is also known as sickle cell disease

Related symptoms:

  • Intellectual disability
  • Pain
  • Anemia
  • Hypertension
  • Hepatomegaly


SOURCES: OMIM MESH ORPHANET MENDELIAN

More info about SICKLE CELL ANEMIA

Low match ATTRV30M AMYLOIDOSIS


Familial amyloid polyneuropathy (FAP) or transthyretin (TTR) amyloid polyneuropathy is a progressive sensorimotor and autonomic neuropathy of adulthood onset. Weight loss and cardiac involvement are frequent; ocular or renal complications may also occur.

ATTRV30M AMYLOIDOSIS Is also known as familial amyloid polyneuropathy type i|ttr amyloid neuropathy|attrv30m-related amyloidosis|hereditary amyloidosis, transthyretin-related|transthyretin amyloid polyneuropathy|familial amyloid polyneuropathy, portuguese-swedish-japanese type|fap|amyloid pol

Related symptoms:

  • Seizures
  • Hearing impairment
  • Ataxia
  • Nystagmus
  • Sensorineural hearing impairment


SOURCES: OMIM ORPHANET MENDELIAN

More info about ATTRV30M AMYLOIDOSIS

Top 5 symptoms//phenotypes associated to Lymphoma and Ischemic stroke

Symptoms // Phenotype % cases
Headache Common - Between 50% and 80% cases
Stroke Common - Between 50% and 80% cases
Splenomegaly Common - Between 50% and 80% cases
Leukemia Common - Between 50% and 80% cases
Hypertension Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

Patients with Lymphoma and Ischemic stroke. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases


Fatigue Vertigo Pain Myelodysplasia Seizures Weight loss Fever Transient ischemic attack Thrombocytosis Venous thrombosis Myocardial infarction Abdominal pain Renal insufficiency Hepatomegaly Intellectual disability Nephropathy Migraine Anemia Recurrent infections Abnormal bleeding Epistaxis Thromboembolism Pruritus Bone marrow hypocellularity Diarrhea Congestive heart failure Cerebral hemorrhage Malabsorption Leukocytosis Cerebral ischemia Respiratory distress Pulmonary embolism Arterial thrombosis Chest pain Neoplasm Paresthesia

Rare Symptoms - Less than 30% cases


Acute myeloid leukemia Abnormal renal physiology Angina pectoris Cough Polycythemia Pulmonary arterial hypertension Ataxia Muscle weakness Hearing impairment Gliosis Hydrocephalus Increased red blood cell mass Hemolytic anemia Reduced bone mineral density Abnormal hemoglobin Cutis marmorata Cardiomegaly Gastrointestinal hemorrhage Polyneuropathy Abnormality of the vasculature Pallor Purpura Multiple cafe-au-lait spots Arthralgia Abnormal thrombosis Gingival bleeding Respiratory insufficiency Visual impairment Chronic myelogenous leukemia Hypercoagulability Peripheral neuropathy Dysarthria Lymphoproliferative disorder Vasculitis Arrhythmia Increased hemoglobin Scoliosis Vomiting Cardiomyopathy Intrauterine growth retardation Depressed nasal bridge Cognitive impairment Growth delay Increased megakaryocyte count Pneumonia Myelofibrosis Myeloproliferative disorder Acute leukemia Syringomyelia Myeloid leukemia Bruising susceptibility Dyspnea Thrombocytopenia Increased hematocrit Dementia Hypothyroidism Autoimmunity Abnormality of the nervous system Arnold-Chiari type I malformation Large earlobe Varicose veins Meningioma Megalencephaly Short lower limbs Capillary hemangioma Severe failure to thrive Displacement of the external urethral meatus Severe postnatal growth retardation Deep venous thrombosis Nevus flammeus Intermittent claudication Abnormality of the lower limb Erythroid hyperplasia Capillary malformation Progressive macrocephaly Telangiectasia of the skin Leukocoria Aplasia/Hypoplasia of the skin Abnormality of digit Hemimegalencephaly Cortical dysplasia Portal vein thrombosis Subcutaneous hemorrhage Vascular ring Portal hypertension Atrial flutter Right aortic arch Skin erosion Aplastic anemia Arterial stenosis Cavum septum pellucidum Dysphagia Dilation of lateral ventricles Hemoglobinuria Hypoplastic anemia Cerebral artery stenosis Asymmetric growth Hyperhidrosis Pancytopenia Blue nevus Syncope Spontaneous abortion Facial hemangioma Abnormality of the upper limb Peripheral arterial stenosis Hemihypertrophy Cutis marmorata telangiectatica congenita Arteriovenous malformation Perisylvian polymicrogyria Erythema Tinnitus Visual field defect Tachypnea Budd-Chiari syndrome Coma Abnormal autonomic nervous system physiology Hallucinations Hemiparesis Bilateral sensorineural hearing impairment Peripheral demyelination Neuronal loss in central nervous system Hypotension Urinary incontinence Peripheral axonal neuropathy Spastic paraparesis Paraplegia Facial palsy Arthritis Constipation Hyporeflexia Areflexia Tremor Spasticity Sensorineural hearing impairment Paraparesis Atrioventricular block Increased red cell sickling tendency Multiple myeloma Cardiac amyloidosis Vitreous floaters Orthostatic hypotension due to autonomic dysfunction Psychomotor deterioration Urinary retention Sensory ataxia Myelopathy Constrictive median neuropathy Stroke-like episode Restrictive cardiomyopathy Cachexia Increased CSF protein Amyloidosis Decreased number of peripheral myelinated nerve fibers Orthostatic hypotension Axonal degeneration Aphasia Malnutrition Impotence Rheumatoid arthritis Nystagmus Pigment gallstones Elevated leukocyte alkaline phosphatase Confusion Nephroblastoma Cerebral palsy Recurrent bacterial infections Bone pain Cholestasis Sepsis Hematuria Hepatic failure Retinopathy Osteomyelitis Irritability Rigidity Jaundice Respiratory failure Osteoporosis Peripheral thrombosis Plethora Exertional dyspnea Myalgia Cholelithiasis Microcytic anemia Priapism Abnormality of the spleen Increased lactate dehydrogenase activity Abnormal lactate dehydrogenase activity Persistence of hemoglobin F Pure red cell aplasia Unconjugated hyperbilirubinemia Chronic hemolytic anemia Hypochromic anemia Microalbuminuria Night sweats Left ventricular failure Wheezing Hypoxemia Increased mean corpuscular volume Atelectasis Asplenia Elevated serum creatinine Reticulocytosis Aseptic necrosis Poor appetite Iron deficiency anemia Large for gestational age Syndactyly Redundant skin Opacification of the corneal stroma Glomerulosclerosis Encephalitis Chronic kidney disease Coarse hair Azoospermia Hyperlipidemia Atherosclerosis Lymphopenia Glomerulonephritis Abnormality of epiphysis morphology Heterotopia Abnormal form of the vertebral bodies Abnormal lung morphology Fine hair Intellectual disability, profound Lumbar hyperlordosis Nephrotic syndrome Epiphyseal dysplasia Nephritis Decreased testicular size Thoracic kyphosis Cellular immunodeficiency Dentinogenesis imperfecta Subvalvular aortic stenosis Precocious atherosclerosis Villous atrophy B-cell lymphoma Disproportionate short-trunk short stature Ovoid vertebral bodies Protuberant abdomen Melanocytic nevus Glomerulopathy Steatorrhea Hypermelanotic macule Combined immunodeficiency High pitched voice Emphysema Focal segmental glomerulosclerosis Spondyloepiphyseal dysplasia Microdontia Waddling gait Arteriosclerosis Abnormality of bone marrow cell morphology Myopia Motor delay Abnormal facial shape Short stature Abnormal platelet aggregation Decreased mean platelet volume Abnormal platelet morphology Bloody diarrhea Amaurosis fugax Cerebellar atrophy Impaired platelet aggregation Abnormal thrombocyte morphology Abnormality of the cerebral vasculature Gangrene Acrocyanosis Prolonged bleeding time Hepatosplenomegaly Abnormality of the skeletal system Short neck Abnormality of the dentition Premature birth Hip dislocation Brain atrophy Abnormal cerebellum morphology Neutropenia Bulbous nose Abnormality of skin pigmentation Stage 5 chronic kidney disease Astigmatism Platyspondyly Corneal opacity Kyphosis Scarring Hyperlordosis Developmental regression Abnormality of the kidney Proteinuria Thin upper lip vermilion Osteopenia Immunodeficiency Right ventricular cardiomyopathy Hypoplasia of the capital femoral epiphysis Arnold-Chiari malformation Patent ductus arteriosus Broad forehead Postnatal growth retardation Joint laxity Deeply set eye High forehead Polydactyly Abnormal heart morphology Hernia Toe syndactyly Abnormality of cardiovascular system morphology Microphthalmia Edema Ventriculomegaly Ventricular septal defect Frontal bossing Downslanted palpebral fissures Macrocephaly Finger syndactyly Smooth philtrum Epicanthus Overgrowth Hemangioma Cutis laxa Cutaneous syndactyly Shock Multicystic kidney dysplasia Telangiectasia Postaxial hand polydactyly Abnormality of the skin Oral cleft Vesicoureteral reflux Nevus Ascites Retinal detachment Thick vermilion border Postaxial polydactyly Polymicrogyria Joint hypermobility Wide nasal bridge Low-set ears Mucopolysacchariduria Anterior pituitary dysgenesis Cranial nerve paralysis Anorexia Memory impairment Lymphadenopathy Proptosis Visual loss Lateral displacement of the femoral head Nephrosclerosis Premature arteriosclerosis Pleural effusion Moyamoya phenomenon Abnormal immunoglobulin level Abnormal T cell morphology Encephalomalacia Increased thyroid-stimulating hormone level Shallow acetabular fossae Steroid-resistant nephrotic syndrome Multiple lentigines Urticaria Elevated erythrocyte sedimentation rate Muscular hypotonia Monoclonal immunoglobulin M proteinemia Micrognathia Failure to thrive Hypertelorism Generalized hypotonia Global developmental delay Polyclonal elevation of IgM Cryoglobulinemia Impaired lymphocyte transformation with phytohemagglutinin Multifocal epileptiform discharges Pulmonary infiltrates Retinal hemorrhage Abnormality of neutrophils Normocytic anemia Periorbital edema Reduced consciousness/confusion Abnormality of the retinal vasculature Edema of the lower limbs Raynaud phenomenon Amyloid deposition in the vitreous humor



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