Lymphoma, and Nephropathy

Diseases related with Lymphoma and Nephropathy

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

Top matches:

Wiskott-Aldrich syndrome (WAS) is a primary immunodeficiency disease characterized by microthrombocytopenia, eczema, infections and an increased risk for autoimmune manifestations and malignancies.

WISKOTT-ALDRICH SYNDROME Is also known as aldrich syndrome|imd2|immunodeficiency 2|eczema-thrombocytopenia-immunodeficiency syndrome|was|was1|wiskott-aldrich syndrome 1

Related symptoms:

  • Neoplasm
  • Anemia
  • Peripheral neuropathy
  • Fever
  • Fatigue


SOURCES: OMIM ORPHANET MENDELIAN

More info about WISKOTT-ALDRICH SYNDROME

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 MULTIPLE MYELOMA

Multiple myeloma (MM) is a malignant tumor of plasma cell characterized by overproduction of abnormal plasma cells in the bone marrow and skeletal destruction. The clinical features are bone pain, renal impairment, immunodeficiency, anemia and presence of abnormal immunoglobulins (Ig).

MULTIPLE MYELOMA Is also known as plasma cell myeloma|myelomatosis|kahler's disease|medullary plasmacytoma

Related symptoms:

  • Neoplasm
  • Anemia
  • Fatigue
  • Splenomegaly
  • Weight loss


SOURCES: ORPHANET OMIM MENDELIAN

More info about MULTIPLE MYELOMA

Other less relevant matches:

Medium match WAGR SYNDROME

WAGR syndrome (Wilms tumor - aniridia - genitourinary anomalies - intellectual disability mental retardation) is a rare genetic disorder characterized by an unusual complex of congenital developmental abnormalities with intellectual disability, and an increased risk of developing Wilms tumor.

WAGR SYNDROME Is also known as del(11)(p13)|chromosome 11p13 deletion syndrome|wilms tumor-aniridia-genitourinary anomalies-intellectual disability syndrome|monosomy 11p13|deletion 11p13|wagr syndrome

Related symptoms:

  • Intellectual disability
  • Short stature
  • Microcephaly
  • Scoliosis
  • Nystagmus


SOURCES: OMIM ORPHANET MENDELIAN

More info about WAGR SYNDROME

Medium 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

Medium 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

Medium match WERNER SYNDROME

Werner syndrome (WS) is a rare inherited syndrome characterized by premature aging with onset in the third decade of life and with cardinal clinical features including bilateral cataracts, short stature, graying and thinning of scalp hair, characteristic skin disorders and premature onset of additional age-related disorders.

WERNER SYNDROME Is also known as ws|adult progeria

Related symptoms:

  • Short stature
  • Neoplasm
  • Pain
  • Cataract
  • Visual impairment


SOURCES: MESH ORPHANET OMIM MENDELIAN

More info about WERNER SYNDROME

Lipoprotein glomerulopathy is an uncommon kidney disease characterized by proteinuria, progressive kidney failure, and distinctive lipoprotein thrombi in glomerular capillaries (Saito et al., 2006). It mainly affects people of Japanese and Chinese origin; in these populations, it is associated with mutations in the gene that encodes apolipoprotein E (APOE ). The disorder had rarely been described in Caucasians.

LIPOPROTEIN GLOMERULOPATHY Is also known as lpg

Related symptoms:

  • Edema
  • Renal insufficiency
  • Carcinoma
  • Proteinuria
  • Abnormality of the kidney


SOURCES: ORPHANET OMIM MESH MENDELIAN

More info about LIPOPROTEIN GLOMERULOPATHY

Familial juvenile hyperuricemic nephropathy type 2 is a rare autosomal dominantly inherited disease of childhood characterized by hypoproliferative anemia, hyperuricemia and slowly progressing kidney failure due to dysregulation of the renin-angiotensin system (RAS).

REN-RELATED AUTOSOMAL DOMINANT TUBULOINTERSTITIAL KIDNEY DISEASE Is also known as early-onset hyperuricemia, anemia, and progressive kidney failure|ren-associated fjhn|ren-associated kidney disease|familial juvenile hyperuricemic nephropathy type 2|ren-associated familial juvenile hyperuricemic nephropathy|adtkd-ren|fjhn type 2

Related symptoms:

  • Anemia
  • Renal insufficiency
  • Stage 5 chronic kidney disease
  • Nephropathy
  • Renal cyst


SOURCES: OMIM MESH ORPHANET MENDELIAN

More info about REN-RELATED AUTOSOMAL DOMINANT TUBULOINTERSTITIAL KIDNEY DISEASE

Denys-Drash syndrome (DDS) is a rare urogenital disorder characterized by the association of diffuse mesangial sclerosis (DMS), male pseudohermaphroditism with a 46,XY karyotype, and nephroblastoma.

DENYS-DRASH SYNDROME Is also known as drash syndrome|wilms tumor-disorder of sex development syndrome|wilms tumor-dsd syndrome

Related symptoms:

  • Neoplasm
  • Hypertension
  • Edema
  • Renal insufficiency
  • Micropenis


SOURCES: OMIM ORPHANET MENDELIAN

More info about DENYS-DRASH SYNDROME

Top 5 symptoms//phenotypes associated to Lymphoma and Nephropathy

Symptoms // Phenotype % cases
Renal insufficiency Common - Between 50% and 80% cases
Neoplasm Uncommon - Between 30% and 50% cases
Anemia Uncommon - Between 30% and 50% cases
Leukemia Uncommon - Between 30% and 50% cases
Proteinuria Uncommon - Between 30% and 50% cases

Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases

Focal segmental glomerulosclerosis Hypertension Fever Visual impairment Congestive heart failure Short stature Chronic kidney disease Glomerulopathy Pain Chest pain Intellectual disability Peripheral neuropathy Recurrent infections Stage 5 chronic kidney disease Glomerulosclerosis Splenomegaly Fatigue Diarrhea Nephrotic syndrome Cardiomyopathy Pneumonia

Rare Symptoms - Less than 30% cases

Amyloidosis Weight loss Cataract Paresthesia Polyneuropathy Nystagmus Scoliosis Increased IgA level Seizures Bone pain Multiple myeloma Elevated serum creatinine Abnormality of the kidney Premature arteriosclerosis Arteriosclerosis Abnormality of the vasculature Atherosclerosis Bone marrow hypocellularity Micropenis Decreased testicular size Carcinoma Migraine Gliosis Malabsorption Vomiting Steroid-resistant nephrotic syndrome Corneal opacity Stroke Coma Osteopenia Dementia Headache Abnormality of the dentition Iron deficiency anemia High pitched voice Microcytic anemia Vasculitis Hemolytic anemia Cough Sarcoma Autoimmunity Rheumatoid arthritis Myeloid leukemia Osteoporosis Arthritis Glomerulonephritis Renal neoplasm Nephroblastoma Retinopathy Neutropenia Sepsis Abnormality of the genitourinary system Abnormality of the genital system Thrombocytopenia Cardiomegaly Edema Gonadoblastoma Immunodeficiency Lymphopenia Combined immunodeficiency Ambiguous genitalia Arrhythmia Skin ulcer Lymphadenopathy Bilateral sensorineural hearing impairment Hypotension Urinary incontinence Peripheral demyelination Neuronal loss in central nervous system Hematuria Paraparesis Hepatic failure Malnutrition Stroke-like episode Restrictive cardiomyopathy Increased CSF protein Syringomyelia Decreased number of peripheral myelinated nerve fibers Orthostatic hypotension Axonal degeneration Aphasia Impotence Hemiparesis Cerebral hemorrhage Cachexia Atrioventricular block Confusion Spastic paraparesis Peripheral axonal neuropathy Abnormal autonomic nervous system physiology Hallucinations Cholestasis Facial palsy Recurrent bacterial infections Abnormal hemoglobin Abnormal lactate dehydrogenase activity Persistence of hemoglobin F Pure red cell aplasia Constrictive median neuropathy Chronic hemolytic anemia Hypochromic anemia Chronic myelogenous leukemia Microalbuminuria Night sweats Priapism Abnormality of the spleen Left ventricular failure Aseptic necrosis Hypoxemia Increased mean corpuscular volume Atelectasis Asplenia Reticulocytosis Increased lactate dehydrogenase activity Pigment gallstones Cerebral palsy Areflexia Paraplegia Tachypnea Cholelithiasis Thrombocytosis Constipation Hyporeflexia Leukocytosis Osteomyelitis Hydrocephalus Increased red cell sickling tendency Wheezing Tremor Poor appetite Dysarthria Spasticity Muscle weakness Sensorineural hearing impairment Ataxia Hearing impairment Unconjugated hyperbilirubinemia Type II diabetes mellitus Myelopathy Meningioma White forelock Slender build Abnormality of the testis Pili torti Chondrocalcinosis Lack of skin elasticity Peripheral arterial stenosis Abnormality of the cerebral vasculature Osteosarcoma Progeroid facial appearance Enlarged joints Posterior subcapsular cataract Pulmonary artery stenosis Neoplasm of the lung Alopecia of scalp Premature loss of teeth Subcapsular cataract Prematurely aged appearance Ovarian neoplasm Secondary amenorrhea Scleroderma Thyroid carcinoma Narrow nasal ridge Aplasia/Hypoplasia of the skin Hyperlipoproteinemia Male pseudohermaphroditism Gonadal dysgenesis Hyperechogenic kidneys Tubulointerstitial fibrosis Tubular atrophy Gout Hyperuricemia Renal hypoplasia Renal cyst Mesangial hypercellularity Renal cell carcinoma Cutaneous melanoma Acral lentiginous melanoma Aplasia/Hypoplasia of the testes Neoplasm of the oral cavity Gastrointestinal carcinoma Neoplasm of the small intestine Subcutaneous calcification Poliosis Abnormal hair whorl Soft tissue sarcoma Chorioretinitis Telangiectasia of the skin Lipoatrophy Abnormal renal physiology Hypogonadism Myocardial infarction Abnormality of the nervous system Convex nasal ridge Hypopigmentation of the skin Small hand Retinal degeneration Joint stiffness Proptosis Hyperkeratosis Diabetes mellitus Rod-cone dystrophy Decreased body weight Alopecia Behavioral abnormality Skeletal muscle atrophy Amyloid deposition in the vitreous humor Cardiac amyloidosis Vitreous floaters Orthostatic hypotension due to autonomic dysfunction Psychomotor deterioration Urinary retention Sensory ataxia Sparse scalp hair Abnormality of retinal pigmentation Decreased fertility Dermal atrophy Polyphagia Premature graying of hair Squamous cell carcinoma Polyuria Rocker bottom foot Abnormality of the thorax Polydipsia Myelodysplasia Abnormality of the voice Lipodystrophy Laryngomalacia Insulin resistance Breast carcinoma Melanoma Macular degeneration Type I diabetes mellitus Spontaneous abortion Hypergonadotropic hypogonadism Hoarse voice Increased bone mineral density Narrow face Abnormality of the hair Irritability Abnormality of vitamin B12 metabolism Rigidity Chronic leukemia Cognitive impairment Abnormal facial shape Growth delay Oral bleeding Specific anti-polysaccharide antibody deficiency Reduced lymphocyte surface expression of CD43 Abnormal delayed hypersensitivity skin test Absent microvilli on the surface of peripheral blood lymphocytes Recurrent intrapulmonary hemorrhage Motor delay Small vessel vasculitis Large vessel vasculitis Reduced delayed hypersensitivity Congenital thrombocytopenia Abnormal platelet morphology Decreased mean platelet volume Abnormal platelet function Internal hemorrhage Abnormal eosinophil morphology Depressed nasal bridge Myopia Bloody diarrhea Astigmatism Lumbar hyperlordosis Microdontia Waddling gait Premature birth Brain atrophy Abnormal cerebellum morphology Bulbous nose Abnormality of skin pigmentation Platyspondyly Intrauterine growth retardation Hip dislocation Scarring Hyperlordosis Developmental regression Thin upper lip vermilion Hypothyroidism Kyphosis Cerebellar atrophy Short neck Generalized lymphadenopathy Spontaneous hematomas Fine hair Epistaxis Intracranial hemorrhage Recurrent upper respiratory tract infections Purpura Conjunctivitis Meningitis Sinusitis Chronic diarrhea Recurrent otitis media Pancytopenia Chronic otitis media Eczema Specific learning disability Otitis media Sudden cardiac death Abnormal bleeding Bruising susceptibility Respiratory tract infection Dyspnea Recurrent respiratory infections Urticaria Inflammation of the large intestine Melena Chronic obstructive pulmonary disease Hematemesis Interstitial pneumonitis Membranoproliferative glomerulonephritis Abnormality of the menstrual cycle Increased IgE level Recurrent ear infections IgM deficiency Hypoplasia of the thymus Hematochezia Hyperostosis Acute leukemia Recurrent lower respiratory tract infections Blepharitis Gingival bleeding Hodgkin lymphoma Cellulitis Prolonged bleeding time Petechiae Keratitis Intellectual disability, profound Abnormal lung morphology Jaundice Increased IgG level Cryptorchidism Micrognathia Microcephaly Plasmacytoma Hyperproteinemia Paraproteinemia Monoclonal immunoglobulin M proteinemia Functional abnormality of the gastrointestinal tract Abnormality of the bladder Microphthalmia Prostate cancer Vertebral compression fractures Neoplasm of the pancreas Spinal cord compression Acute kidney injury Abnormality of blood and blood-forming tissues Pathologic fracture Colon cancer Increased antibody level in blood Ptosis Obesity Hypercalcemia Abnormal vagina morphology Respiratory failure Abdominal pain Respiratory distress Hepatomegaly Dysfunction of lateral corticospinal tracts Displacement of the external urethral meatus Streak ovary Aplasia/Hypoplasia of the iris Peters anomaly Hypospadias Abnormality of the uterus Hemihypertrophy Hearing abnormality Acute lymphoblastic leukemia Aniridia Microcornea Everted lower lip vermilion Hypertrophic cardiomyopathy Glaucoma Pleural effusion Tall stature Abnormal form of the vertebral bodies Melanocytic nevus Thoracic kyphosis Transient ischemic attack Protuberant abdomen Multiple cafe-au-lait spots Steatorrhea Hypermelanotic macule Emphysema Spondyloepiphyseal dysplasia Nephritis Disproportionate short-trunk short stature Epiphyseal dysplasia Encephalitis Coarse hair Reduced bone mineral density Azoospermia Hyperlipidemia Opacification of the corneal stroma Abnormality of epiphysis morphology Heterotopia Ovoid vertebral bodies B-cell lymphoma Decreased antibody level in blood Shallow acetabular fossae Generalized muscle weakness Lateral displacement of the femoral head Nephrosclerosis Anterior pituitary dysgenesis Moyamoya phenomenon Abnormal immunoglobulin level Abnormal T cell morphology Encephalomalacia Increased thyroid-stimulating hormone level Multiple lentigines Lymphoproliferative disorder Mucopolysacchariduria Hypoplasia of the capital femoral epiphysis Right ventricular cardiomyopathy Cellular immunodeficiency Dentinogenesis imperfecta Subvalvular aortic stenosis Precocious atherosclerosis Cerebral ischemia Villous atrophy Diffuse mesangial sclerosis


If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like Hepatomegaly and Abdominal pain, related diseases and genetic alterations Congestive heart failure and Dandy-Walker malformation, related diseases and genetic alterations