Lymphoma, and Fatigue

Diseases related with Lymphoma and Fatigue

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


Top matches:

Medium match MANTLE CELL LYMPHOMA


Mantle cell lymphoma is a rare form of malignant non-Hodgkin lymphoma (see this term) affecting B lymphocytes in the lymph nodes in a region called the ``mantle zone''.

MANTLE CELL LYMPHOMA Is also known as mantle zone lymphoma|lcm|mcl

Related symptoms:

  • Neoplasm
  • Fever
  • Fatigue
  • Splenomegaly
  • Weight loss


SOURCES: ORPHANET MENDELIAN

More info about MANTLE CELL LYMPHOMA

Medium match OVARIAN CANCER


Ovarian cancer, the leading cause of death from gynecologic malignancy, is characterized by advanced presentation with loco-regional dissemination in the peritoneal cavity and the rare incidence of visceral metastases (Chi et al., 2001). These typical features relate to the biology of the disease, which is a principal determinant of outcome (Auersperg et al., 2001). Epithelial ovarian cancer is the most common form and encompasses 5 major histologic subtypes: papillary serous, endometrioid, mucinous, clear cell, and transitional cell. Epithelial ovarian cancer arises as a result of genetic alterations sustained by the ovarian surface epithelium (Stany et al., 2008; Soslow, 2008).

Related symptoms:

  • Neoplasm
  • Pain
  • Fatigue
  • Respiratory distress
  • Vomiting


SOURCES: OMIM ORPHANET MENDELIAN

More info about OVARIAN CANCER

Medium match FOLLICULAR LYMPHOMA


Follicular lymphoma is a form of non-Hodgkin lymphoma (see this term) characterized by a proliferation of B cells whose nodular structure of follicular architecture is preserved.

FOLLICULAR LYMPHOMA Is also known as oncogene b-cell leukemia 2

Related symptoms:

  • Neoplasm
  • Fever
  • Fatigue
  • Diarrhea
  • Splenomegaly


SOURCES: OMIM ORPHANET MENDELIAN

More info about FOLLICULAR LYMPHOMA

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Other less relevant matches:

Medium match MALT LYMPHOMA


MALT (mucosa-associated lymphoid tissue) lymphoma is a rare form of malignant non-Hodgkin lymphoma (see this term) that affects B cells and grows at the expense of lymphoid tissue associated with mucous membranes, but also occurs, more rarely, in lymph nodes.

MALT LYMPHOMA Is also known as maltoma|mucosa-associated lymphatic tissue lymphoma|extranodal marginal zone b-cell lymphoma|mucosa-associated lymphoid tissue lymphoma

Related symptoms:

  • Anemia
  • Visual impairment
  • Fever
  • Fatigue
  • Constipation


SOURCES: ORPHANET MENDELIAN

More info about MALT LYMPHOMA

Medium match ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY


G6PD deficiency is the most common genetic cause of chronic and drug-, food-, or infection-induced hemolytic anemia. G6PD catalyzes the first reaction in the pentose phosphate pathway, which is the only NADPH-generation process in mature red cells; therefore, defense against oxidative damage is dependent on G6PD. Most G6PD-deficient patients are asymptomatic throughout their life, but G6PD deficiency can be life-threatening. The most common clinical manifestations of G6PD deficiency are neonatal jaundice and acute hemolytic anemia, which in most patients is triggered by an exogenous agent, e.g., primaquine or fava beans. Acute hemolysis is characterized by fatigue, back pain, anemia, and jaundice. Increased unconjugated bilirubin, lactate dehydrogenase, and reticulocytosis are markers of the disorder. The striking similarity between the areas where G6PD deficiency is common and Plasmodium falciparum malaria (see {611162}) is endemic provided evidence that G6PD deficiency confers resistance against malaria (summary by Cappellini and Fiorelli, 2008).

ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY Is also known as favism, susceptibility to

Related symptoms:

  • Intellectual disability
  • Neoplasm
  • Muscle weakness
  • Pain
  • Anemia


SOURCES: OMIM MENDELIAN

More info about ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY

Medium match CHRONIC EPSTEIN-BARR VIRUS INFECTION SYNDROME


Chronic Epstein-Barr virus infection syndrome is a rare infectious disease characterized by familial, primary, chronic Epstein-Barr virus infection which typically manifests with persistent mononucleosis-like signs and symptoms, in the absence of secondary immunodeficiency.

CHRONIC EPSTEIN-BARR VIRUS INFECTION SYNDROME Is also known as irf8 deficiency, autosomal recessive|epstein-barr virus, susceptibility to chronic infection by|immunodeficiency 32b, monocyte, dendritic cell, and natural killer cell deficiency, autosomal recessive|caebv syndrome|chronic ebv infection syndrome

Related symptoms:

  • Global developmental delay
  • Neoplasm
  • Failure to thrive
  • Anemia
  • Hepatomegaly


SOURCES: ORPHANET OMIM MENDELIAN

More info about CHRONIC EPSTEIN-BARR VIRUS INFECTION SYNDROME

Medium match HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES


Hereditary neuropathy with liability to pressure palsies (HNPP) is an inherited peripheral nerve disorder characterized by recurrent mononeuropathy usually triggered by minor physical activities.

HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES Is also known as hnpp|potato-grubbing palsy|polyneuropathy, familial recurrent|current pressure-sensitive neuropathy|heterozygous microdeletion 17p11.2p12|tulip-bulb digger's palsy|tomaculous neuropathy

Related symptoms:

  • Hearing impairment
  • Scoliosis
  • Muscle weakness
  • Pain
  • Peripheral neuropathy


SOURCES: OMIM MESH ORPHANET MENDELIAN

More info about HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES

Medium match LYMPHOMA, HODGKIN, CLASSIC; CHL


Classic Hodgkin lymphoma is a lymph node cancer of germinal center B-cell origin. Hodgkin lymphoma tumors consist of a minority of malignant cells, known as 'Reed-Sternberg' (RS) cells, mixed with reactive lymphocytes and other benign inflammatory cells. A defining feature of RS cells is the presence of 2 nuclei (summary by Salipante et al., 2009).

LYMPHOMA, HODGKIN, CLASSIC; CHL Is also known as hodgkin disease

Related symptoms:

  • Ataxia
  • Neoplasm
  • Peripheral neuropathy
  • Hepatomegaly
  • Fever


SOURCES: OMIM ORPHANET MENDELIAN

More info about LYMPHOMA, HODGKIN, CLASSIC; CHL

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

Medium match CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1


Celiac disease, also known as celiac sprue and gluten-sensitive enteropathy (GSE), is a multifactorial disorder of the small intestine that is influenced by both environmental and genetic factors. It is characterized by malabsorption resulting from inflammatory injury to the mucosa of the small intestine after the ingestion of wheat gluten or related rye and barley proteins (summary by Farrell and Kelly, 2002). Long regarded as gastrointestinal disorder of childhood, the disease is now considered to be a chronic systemic autoimmune disease and is more often diagnosed in adults than in children (Monsuur et al., 2005).For a discussion of genetic heterogeneity of celiac disease, see MAPPING.

CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1 Is also known as celiac sprue, susceptibility to, 1|gluten-sensitive enteropathy, susceptibility to, 1

Related symptoms:

  • Seizures
  • Short stature
  • Ataxia
  • Failure to thrive
  • Anemia


SOURCES: OMIM MENDELIAN

More info about CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1

Top 5 symptoms//phenotypes associated to Lymphoma and Fatigue

Symptoms // Phenotype % cases
Weight loss Common - Between 50% and 80% cases
Neoplasm Common - Between 50% and 80% cases
Fever Common - Between 50% and 80% cases
Lymphadenopathy Common - Between 50% and 80% cases
Anemia Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases


Hodgkin lymphoma Splenomegaly Pain Abdominal pain Skin rash Diarrhea Back pain B-cell lymphoma

Rare Symptoms - Less than 30% cases


Polyneuropathy Cellular immunodeficiency Leukemia Lymphedema Meningitis Immunodeficiency Skin nodule Hepatomegaly Recurrent respiratory infections Hyperhidrosis Respiratory insufficiency Peripheral neuropathy Muscle weakness Pneumonia Mediastinal lymphadenopathy Respiratory tract infection Failure to thrive Nausea Anorexia Abnormality of the gastrointestinal tract Night sweats Vomiting Constipation Nausea and vomiting Ataxia Abdominal distention Migraine Bone pain Abnormal lung morphology Neoplasm of the skin Hemangioma Sarcoma Hypermelanotic macule Abnormal retinal morphology Macule Segmental peripheral demyelination/remyelination Vocal cord paresis Abnormality of the lower limb Lymphoproliferative disorder Abnormality of the spleen Poor appetite Bone marrow hypocellularity Pulmonary arterial hypertension Gastrointestinal hemorrhage Monoclonal immunoglobulin M proteinemia Edema Venous insufficiency Chest pain Impaired lymphocyte transformation with phytohemagglutinin Polyclonal elevation of IgM Hypertension Pruritus Cough Myelin tomacula Encephalopathy Lung adenocarcinoma Osteolysis Abnormality of the liver Brachial plexus neuropathy Papule Hemoptysis Malabsorption Generalized lymphadenopathy Iron deficiency anemia Abnormal intestine morphology Rickets Abnormality of the coagulation cascade Malnutrition Steatorrhea Celiac disease Macrocytic anemia IgA deficiency Thyroiditis Thrombocytosis Type I diabetes mellitus Chronic fatigue Prolonged partial thromboplastin time Stomatitis Recurrent aphthous stomatitis Prolonged prothrombin time Abnormality of the abdominal wall Folate deficiency Vitamin D deficiency Vitamin K deficiency Spontaneous abortion Hypocalcemia Skin plaque Anxiety Susceptibility to herpesvirus Neoplasm by anatomical site Seizures Short stature Depressivity Alopecia Osteoporosis Arthralgia Elevated hepatic transaminase Irritability Chronic diarrhea Postnatal growth retardation Autoimmunity Low back pain Delayed puberty Infertility Nevus Cerebral calcification Eczema Inflammatory abnormality of the skin Hypoplasia of dental enamel Abnormal myelination Confusion Constrictive median neuropathy Myalgia Abnormality of the peritoneum Visual impairment Abnormality of the thyroid gland Pulmonary infiltrates Abnormal nasolacrimal system morphology Posterior uveitis Intellectual disability Jaundice Pallor Glucose intolerance Cirrhosis Hemolytic anemia Abnormality of the cardiovascular system Hyperbilirubinemia Leukocytosis Osteomyelitis Prolonged neonatal jaundice Reticulocytosis Chronic lymphatic leukemia Pleural effusion Poikilocytosis Ascites Intestinal polyposis Abnormality of bone marrow cell morphology Intestinal polyp Intussusception Respiratory distress Abnormality of metabolism/homeostasis Gastroesophageal reflux Carcinoma Increased body weight Insulin resistance Melanoma Breast carcinoma Ovarian neoplasm Ovarian carcinoma Dysgerminoma Non-Hodgkin lymphoma Ovarian papillary adenocarcinoma Neutropenia Anisocytosis Hemoglobinuria Vocal cord paralysis Hypotelorism Paralysis Abnormality of movement Paresthesia Inability to walk Sensory neuropathy Muscle cramps Generalized muscle weakness Peripheral demyelination Tetraparesis Myoclonus Hoarse voice Foot dorsiflexor weakness Cranial nerve paralysis Abnormality of the voice Hammertoe Decreased motor nerve conduction velocity Axonal degeneration Axonal loss Abnormality of the nervous system Pes cavus Nonspherocytic hemolytic anemia Hepatic failure Unconjugated hyperbilirubinemia Kernicterus Fava bean-induced hemolytic anemia Global developmental delay Dilatation Recurrent infections Thrombocytopenia Respiratory failure Bronchiectasis Hyporeflexia Sinusitis Recurrent pneumonia Recurrent sinusitis Chronic infection Hearing impairment Scoliosis Skeletal muscle atrophy Areflexia Vitamin B12 deficiency



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