Lymphoma, and Memory impairment

Diseases related with Lymphoma and Memory impairment

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


Top matches:

Medium match X-LINKED LYMPHOPROLIFERATIVE DISEASE


X-linked lymphoproliferative disease is a hereditary immunodeficiency characterized, in the majority of cases, by an inadequate immune response to infection with the Epstein-Barr virus (EBV).

X-LINKED LYMPHOPROLIFERATIVE DISEASE Is also known as xlpd|duncan disease|xlp|immunodeficiency 5|infectious mononucleosis, severe, susceptibility to|purtilo syndrome|imd5|ebvs|lymphoproliferative disease, x-linked|epstein-barr virus infection, familial fatal|lyp|ebv infection, severe, susceptibility to|immun

Related symptoms:

  • Seizures
  • Neoplasm
  • Anemia
  • Hepatomegaly
  • Fever


SOURCES: ORPHANET OMIM MENDELIAN

More info about X-LINKED LYMPHOPROLIFERATIVE DISEASE

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

Low match NASU-HAKOLA DISEASE


Nasu-Hakola disease (NHD), also referred to as polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (PLOSL), is a rare inherited leukodystrophy characterized by progressive presenile dementia associated with recurrent bone fractures due to polycystic osseous lesions of the lower and upper extremities.

NASU-HAKOLA DISEASE Is also known as plosl|dementia, prefrontal, with bone cysts|plo-sl|dementia, progressive, with lipomembranous polycystic osteodysplasia|nasu-hakola disease|polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy|brain-bone-fat disease|nhd|presenile d

Related symptoms:

  • Seizures
  • Pain
  • Spasticity
  • Gait disturbance
  • Ventriculomegaly


SOURCES: ORPHANET MESH OMIM MENDELIAN

More info about NASU-HAKOLA DISEASE

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Other less relevant matches:

Low match PGM3-CDG


PGM3-CDG is a rare congenital disorder of glycosylation caused by mutations in the PGM3 gene and characterized by neonatal to childhood onset of recurrent bacterial and viral infections, inflammatory skin diseases, atopic dermatitis and atopic diatheses, and marked serum IgE elevation. Early neurologic impairment is evident including developmental delay, intellectual disability, ataxia, dysarthria, sensorineural hearing loss, myoclonus and seizures.

PGM3-CDG Is also known as cid due to pgm3 deficiency|immunodeficiency with hyper ige and cognitive impairment|pgm3-related congenital disorder of glycosylation|combined immunodeficiency due to pgm3 deficiency|immunodeficiency-vasculitis-myoclonus syndrome|ivms

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Generalized hypotonia


SOURCES: OMIM ORPHANET MENDELIAN

More info about PGM3-CDG

Low match CHÉDIAK-HIGASHI SYNDROME


Chédiak-Higashi syndrome (CHS) is a rare severe genetic disorder generally characterized by partial oculocutaneous albinism (OCA, see this term), severe immunodeficiency, mild bleeding, neurological dysfunction and lymphoproliferative disorder. A classic, early-onset form and an attenuated, later-onset form (Atypical CHS; see this term) have been described.

CHÉDIAK-HIGASHI SYNDROME Is also known as chÉdiak-higashi-steinbrink syndrome|chÉdiak-higashi disease

Related symptoms:

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


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about CHÉDIAK-HIGASHI SYNDROME

Low match GROWTH DELAY DUE TO INSULIN-LIKE GROWTH FACTOR I RESISTANCE


Growth delay due to IGF-I resistance is characterised by variable intrauterine and postnatal growth retardation and elevated serum IGF-I levels. Addition features include variable degrees of intellectual deficit, microcephaly and dysmorphism (broad nasal bridge and tip, smooth philtrum, thin upper and everted lower lips, short fingers, clinodactyly, wide-set nipples and pectus excavatum).

GROWTH DELAY DUE TO INSULIN-LIKE GROWTH FACTOR I RESISTANCE Is also known as igf-i resistance|resistance to igf-1|somatomedin, end-organ insensitivity to|somatomedin-c, resistance to

Related symptoms:

  • Intellectual disability
  • Global developmental delay
  • Short stature
  • Generalized hypotonia
  • Microcephaly


SOURCES: ORPHANET OMIM MENDELIAN

More info about GROWTH DELAY DUE TO INSULIN-LIKE GROWTH FACTOR I RESISTANCE

Low match NIJMEGEN BREAKAGE SYNDROME


Nijmegen breakage syndrome is a rare genetic disease presenting at birth with microcephaly, dysmorphic facial features, becoming more noticeable with age, growth delay, and later-onset complications such as malignancies and infections.

NIJMEGEN BREAKAGE SYNDROME Is also known as microcephaly-immunodeficiency-lymphoreticuloma syndrome|ataxia-telangiectasia variant v1|microcephaly with normal intelligence, immunodeficiency, and lymphoreticular malignancies|at-v1|berlin breakage syndrome|ataxia-telangiectasia, variant 1|seemanova sy

Related symptoms:

  • Intellectual disability
  • Global developmental delay
  • Short stature
  • Microcephaly
  • Ataxia


SOURCES: ORPHANET OMIM MESH MENDELIAN

More info about NIJMEGEN BREAKAGE SYNDROME

Low match ATAXIA-TELANGIECTASIA


Ataxia-telangiectasia is the association of severe combined immunodeficiency (affecting mainly the humoral immune response) with progressive cerebellar ataxia. It is characterised by neurological signs, telangiectasias, increased susceptibility to infections and a higher risk of cancer.

ATAXIA-TELANGIECTASIA Is also known as at1|louis-bar syndrome

Related symptoms:

  • Intellectual disability
  • Seizures
  • Short stature
  • Microcephaly
  • Scoliosis


SOURCES: ORPHANET OMIM MENDELIAN

More info about ATAXIA-TELANGIECTASIA

Low 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

Top 5 symptoms//phenotypes associated to Lymphoma and Memory impairment

Symptoms // Phenotype % cases
Seizures Common - Between 50% and 80% cases
Intellectual disability Common - Between 50% and 80% cases
Anemia Common - Between 50% and 80% cases
Immunodeficiency Common - Between 50% and 80% cases
Ataxia Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases


Recurrent infections Leukemia Short stature Neoplasm Lymphopenia Recurrent respiratory infections Global developmental delay Thrombocytopenia Combined immunodeficiency Pneumonia B-cell lymphoma Fever Cognitive impairment Bronchiectasis Cerebellar atrophy Diarrhea Peripheral neuropathy Myoclonus Microcephaly Growth delay Skeletal muscle atrophy Lymphoproliferative disorder Strabismus Developmental regression Neutropenia Intrauterine growth retardation Failure to thrive Scoliosis Abnormality of movement Generalized hypotonia Abnormal facial shape Gait disturbance Cafe-au-lait spot Lymphadenopathy Vasculitis Cellular immunodeficiency Hepatomegaly Splenomegaly Multiple cafe-au-lait spots Pancytopenia

Rare Symptoms - Less than 30% cases


Recurrent pneumonia Acute lymphoblastic leukemia Upslanted palpebral fissure Abnormality of the hair Recurrent bronchitis High palate Dysarthria Sinusitis Abnormality of chromosome stability Acute leukemia Telangiectasia Reduced bone mineral density Oculomotor apraxia Abnormality of epiphysis morphology Apraxia Peripheral demyelination Chorea Gliosis Abnormal cerebellum morphology Neurological speech impairment Dementia Edema Hyporeflexia Hemolytic anemia Abnormality of the nervous system Mental deterioration Micrognathia Retrognathia Spinocerebellar tract degeneration Hypopigmentation of hair Resting tremor Melanocytic nevus Cutaneous photosensitivity Brain atrophy Hypoplasia of the corpus callosum Thin upper lip vermilion Anxiety Difficulty walking Respiratory tract infection Small for gestational age Type II diabetes mellitus Tremor High pitched voice Nystagmus Severe combined immunodeficiency Muscle weakness Glomerulonephritis Leukopenia Depressed nasal bridge Short neck Diabetes mellitus Neurodegeneration Motor delay Cranial nerve paralysis Migraine Autoimmunity Stroke Malabsorption Headache Renal insufficiency Congestive heart failure Burkitt lymphoma Polyneuropathy Respiratory insufficiency Decreased antibody level in blood Falls Non-Hodgkin lymphoma Bone marrow hypocellularity Respiratory failure Spasticity Epistaxis Hearing impairment Encephalitis Dysgammaglobulinemia Hodgkin lymphoma Gingival bleeding Gastrointestinal hemorrhage Hepatosplenomegaly Penoscrotal hypospadias Recurrent infection of the gastrointestinal tract Malar prominence Mastoiditis Progressive vitiligo Flexion contracture Dystonia T-cell lymphoma Gait ataxia Anorectal anomaly Elevated hepatic transaminase Ventriculomegaly Carcinoma Abnormal vertebral morphology Premature graying of hair Glucose intolerance Athetosis Spinal muscular atrophy Polycystic ovaries Slurred speech Breast carcinoma Cerebral palsy Reduced tendon reflexes Truncal ataxia Limb ataxia Abnormality of the liver Choreoathetosis Intention tremor Hepatitis Progressive cerebellar ataxia Dilatation Distal amyotrophy Pollakisuria Abnormality of eye movement Delayed puberty Distal muscle weakness Unsteady gait Glioma B lymphocytopenia Hydronephrosis Sloping forehead Amenorrhea Convex nasal ridge Otitis media Prominent nose Cleft upper lip Anal atresia Prominent nasal bridge Attention deficit hyperactivity disorder Intellectual disability, moderate Macrotia Choanal atresia Hyperactivity Hypospadias Cleft palate Sarcoma Increased serum insulin-like growth factor 1 Hypoplastic facial bones Prominent scalp veins Rieger anomaly Broad finger Esodeviation Perimembranous ventricular septal defect Primary amenorrhea Abnormality of the face Decrease in T cell count Abnormality of the musculature Abnormal hair quantity Rhabdomyosarcoma Telangiectasia of the skin Medulloblastoma Recurrent sinopulmonary infections Abnormal eyelid morphology Hearing abnormality Anal stenosis Neuroblastoma Autoimmune hemolytic anemia Freckling Recurrent urinary tract infections Long nose Non-midline cleft lip Abnormality of neuronal migration Premature ovarian insufficiency Deep philtrum Cachexia Hepatic failure Low anterior hairline Hemiparesis Meningitis Chronic diarrhea Aplasia/Hypoplasia of the skin Renal neoplasm Abnormality of the immune system Chronic kidney disease Glomerulopathy Steatorrhea Hypermelanotic macule Emphysema Focal segmental glomerulosclerosis Spondyloepiphyseal dysplasia Nephritis Epiphyseal dysplasia Glomerulosclerosis Coarse hair Abnormality of the vasculature Azoospermia Hyperlipidemia Atherosclerosis Opacification of the corneal stroma Heterotopia Abnormal form of the vertebral bodies Abnormal lung morphology Fine hair Intellectual disability, profound Lumbar hyperlordosis Protuberant abdomen Transient ischemic attack Microdontia Multiple lentigines Nephrosclerosis Anterior pituitary dysgenesis Premature arteriosclerosis Moyamoya phenomenon Abnormal immunoglobulin level Abnormal T cell morphology Encephalomalacia Increased thyroid-stimulating hormone level Shallow acetabular fossae Steroid-resistant nephrotic syndrome Mucopolysacchariduria Thoracic kyphosis Hypoplasia of the capital femoral epiphysis Arteriosclerosis Right ventricular cardiomyopathy Dentinogenesis imperfecta Subvalvular aortic stenosis Precocious atherosclerosis Cerebral ischemia Villous atrophy Disproportionate short-trunk short stature Ovoid vertebral bodies Nephrotic syndrome Decreased testicular size Myeloid leukemia Chronic myelogenous leukemia Progressive spinal muscular atrophy Mucosal telangiectasiae Aplasia/Hypoplasia of the thymus Increased sensitivity to ionizing radiation Female hypogonadism Chronic hepatitis Decreased proportion of CD4-positive T cells Elevated alpha-fetoprotein Abnormal spermatogenesis Neoplasm of the breast Conjunctival telangiectasia Decreased/absent ankle reflexes Chronic lymphatic leukemia Hypoplasia of the thymus Absent Achilles reflex Abnormality of the testis Small face Chromosome breakage Recurrent lower respiratory tract infections Hepatocellular carcinoma IgA deficiency Prematurely aged appearance Immunoglobulin IgG2 deficiency Interosseus muscle atrophy Waddling gait Hyperlordosis Premature birth Nephropathy Bulbous nose Abnormality of skin pigmentation Stage 5 chronic kidney disease Astigmatism Platyspondyly Hip dislocation Corneal opacity Scarring Abnormality of the kidney IgE deficiency Proteinuria Osteopenia Hypothyroidism Kyphosis Abnormality of the dentition Vomiting Cardiomyopathy Myopia Hypertension Defective B cell differentiation Abnormality of the rib cage Radial deviation of finger Maternal diabetes Gastroesophageal reflux Recurrent skin infections Narrow palpebral fissure Inflammatory abnormality of the skin Eczema Sensory impairment Asthma Vertigo Erythema Conductive hearing impairment Anorexia Atopic dermatitis Abnormality of the skeletal system Brachydactyly Purpura Urticaria Pleural effusion Sensorineural hearing impairment Cutis marmorata Elevated erythrocyte sedimentation rate Pulmonary infiltrates Raynaud phenomenon Pallor Proptosis Euphoria Photophobia Sensory neuropathy Bruising susceptibility Peripheral axonal neuropathy Paresthesia Paraplegia Spastic paraplegia Abnormality of the eye Fatigue Rigidity Jaundice Allergic rhinitis Reduced visual acuity Areflexia Atrial septal defect Visual impairment Visual loss Weight loss Cortical myoclonus Autoimmune neutropenia Vasculitis in the skin Membranoproliferative glomerulonephritis Edema of the lower limbs Lack of insight Abnormal bleeding Irritability Cerebral calcification Abnormality of neutrophils Urinary incontinence Limitation of joint mobility Retinal hemorrhage Multifocal epileptiform discharges Monoclonal immunoglobulin M proteinemia Abnormality of the foot Impaired lymphocyte transformation with phytohemagglutinin Cryoglobulinemia Periorbital edema Aggressive behavior EEG abnormality Arthralgia Skeletal dysplasia Cerebral cortical atrophy Polyclonal elevation of IgM Pain Babinski sign Cerebral atrophy Behavioral abnormality Normocytic anemia Bone pain Abnormal adipose tissue morphology Cerebral edema Caudate atrophy Functional abnormality of the gastrointestinal tract Frontal lobe dementia Agnosia Abnormal upper motor neuron morphology Inappropriate behavior Primitive reflex Bone cyst Disinhibition Senile plaques Reduced consciousness/confusion Hypercoagulability Neurofibrillary tangles Axonal loss Basal ganglia calcification Pathologic fracture Alzheimer disease Personality changes Abnormality of the hand Abnormality of the retinal vasculature Leukoencephalopathy Hypopigmentation of the skin Parkinsonism Severe failure to thrive Synophrys Short foot Highly arched eyebrow Everted lower lip vermilion Small hand Inability to walk Short distal phalanx of finger Short palm Thin vermilion border Smooth philtrum Aplastic anemia Triangular face Postnatal growth retardation Muscular hypotonia of the trunk Immune dysregulation Deeply set eye Recurrent pharyngitis Lymphocytosis Narrow mouth Histiocytosis Hepatic encephalopathy Severe short stature Delayed eruption of teeth Broad nasal tip Clinodactyly Pterygium Severe intrauterine growth retardation Increased antibody level in blood Reduced subcutaneous adipose tissue Truncal obesity Delayed cranial suture closure Agitation Hydrocephalus Lipodystrophy Patent foramen ovale Acanthosis nigricans Webbed neck Sandal gap Accelerated skeletal maturation Finger clinodactyly IgG deficiency Decreased body weight Sparse scalp hair Blue sclerae Epidermal acanthosis Agammaglobulinemia Wide intermamillary distance Delayed skeletal maturation Pectus excavatum Fulminant hepatitis Albinism White hair Generalized hypopigmentation Fair hair Periodontitis Gingivitis Iris hypopigmentation Generalized hyperpigmentation Sensory axonal neuropathy Cerebral hemorrhage Pharyngitis Hemophagocytosis Decreased nerve conduction velocity Abnormality of vision Foot dorsiflexor weakness Skin ulcer Hyperpigmentation of the skin Amblyopia Hypertriglyceridemia Reduced natural killer cell activity Abnormality of extrapyramidal motor function Bradykinesia Hepatic necrosis Progressive peripheral neuropathy Obesity Pure red cell aplasia Malar flattening Long philtrum Hypertonia Ventricular septal defect Granulomatosis Wide nasal bridge Chorioretinitis Delayed speech and language development Low-set ears Increased IgM level Generalized hypopigmentation of hair Hypersplenism Recurrent systemic pyogenic infections Abnormality of multiple cell lineages in the bone marrow Giant melanosomes in melanocytes Recurrent cutaneous abscess formation Abnormal leukocyte morphology Hypofibrinogenemia Oculogyric crisis Recurrent bacterial skin infections Macular hypoplasia Partial albinism Lateral displacement of the femoral head



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