Lymphoma, and Congestive heart failure

Diseases related with Lymphoma and Congestive heart failure

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

Top matches:

Low match WHIM SYNDROME

WHIM (warts, hypogammaglobulinemia, infections, and myelokathexis) syndrome is a congenital autosomal dominant immune deficiency characterized by abnormal retention of mature neutrophils in the bone marrow (myelokathexis) and occasional hypogammaglobulinemia, associated with an increased risk for bacterial infections and a susceptibility to human papillomavirus (HPV) induced lesions (cutaneous warts, genital dysplasia and invasive mucosal carcinoma).

WHIM SYNDROME Is also known as warts, hypogammaglobulinemia, infections, and myelokathexis syndrome|warts-infections-leukopenia-myelokatexis syndrome|wilm|warts-hypogammaglobulinemia-infections-myelokathexis syndrome

Related symptoms:

  • Hearing impairment
  • Neoplasm
  • Fever
  • Congestive heart failure
  • Immunodeficiency


SOURCES: MESH OMIM ORPHANET MENDELIAN

More info about WHIM SYNDROME

Common variable immunodeficiency-8 with autoimmunity is an autosomal recessive disorder of immune dysregulation. Affected individuals have early childhood onset of recurrent infections, particularly respiratory infections, and also develop variable autoimmune disorders, including idiopathic thrombocytopenic purpura, autoimmune hemolytic anemia, and inflammatory bowel disease. The presentation and phenotype are highly variable, even within families (summary by Lopez-Herrera et al., 2012 and Alangari et al., 2012). Immunologic findings are also variable and may include decreased B cells, hypogammaglobulinemia, and deficiency of CD4+ T regulatory (Treg) cells (Charbonnier et al., 2015).For a general description and a discussion of genetic heterogeneity of common variable immunodeficiency, see CVID1 (OMIM ).

COMBINED IMMUNODEFICIENCY DUE TO LRBA DEFICIENCY Is also known as cid due to lrba deficiency

Related symptoms:

  • Growth delay
  • Neoplasm
  • Failure to thrive
  • Anemia
  • Diarrhea


SOURCES: OMIM ORPHANET MENDELIAN

More info about COMBINED IMMUNODEFICIENCY DUE TO LRBA DEFICIENCY

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

Other less relevant matches:

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

Low match FANCONI ANEMIA

Fanconi anemia (FA) is a hereditary DNA repair disorder characterized by progressive pancytopenia with bone marrow failure, variable congenital malformations and predisposition to develop hematological or solid tumors.

FANCONI ANEMIA Is also known as fanconi pancytopenia|fanconi anemia|fa

Related symptoms:

  • Intellectual disability
  • Global developmental delay
  • Short stature
  • Hearing impairment
  • Microcephaly


SOURCES: OMIM ORPHANET MENDELIAN

More info about FANCONI ANEMIA

Cardiofaciocutaneous (CFC) syndrome is a RASopathy characterized by craniofacial dysmorphology, congenital heart disease, dermatological abnormalities (most commonly hyperkeratotic skin and sparse, curly hair), growth retardation and intellectual disability.

CARDIOFACIOCUTANEOUS SYNDROME Is also known as cfcs|cfc syndrome

Related symptoms:

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


SOURCES: ORPHANET OMIM MENDELIAN

More info about CARDIOFACIOCUTANEOUS SYNDROME

Congenital dyserythropoietic anemia type II (CDA II) is the most common form of CDA (see this term) characterized by anemia, jaundice and splenomegaly and often leading to liver iron overload and gallstones.

CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE II Is also known as dyserythropoietic anemia, congenital, type ii|cda ii|sec23b-cdg|hempas|hereditary erythroblastic multinuclearity with positive acidified-serum test|cda type ii|cda type 2|hereditary erythroblastic multinuclearity with a positive acidified-serum test (hemp

Related symptoms:

  • Anemia
  • Hepatomegaly
  • Congestive heart failure
  • Splenomegaly
  • Arrhythmia


SOURCES: ORPHANET OMIM MENDELIAN

More info about CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE II

POLYHYDRAMNIOS-MEGALENCEPHALY-SYMPTOMATIC EPILEPSY SYNDROME Is also known as pmse syndrome

Related symptoms:

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


SOURCES: MESH OMIM ORPHANET MENDELIAN

More info about POLYHYDRAMNIOS-MEGALENCEPHALY-SYMPTOMATIC EPILEPSY SYNDROME

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

Thiamine-responsive megaloblastic anemia (TRMA) is characterized by a triad of megaloblastic anemia, non-type I diabetes mellitus, and sensorineural deafness.

THIAMINE-RESPONSIVE MEGALOBLASTIC ANEMIA SYNDROME Is also known as thmd1|trma|thiamine-responsive megaloblastic anemia with diabetes mellitus and sensorineural deafness|rogers syndrome|thiamine-responsive myelodysplasia|thiamine metabolism dysfunction syndrome 1 (megaloblastic anemia, diabetes mellitus, and deafness type

Related symptoms:

  • Seizures
  • Global developmental delay
  • Short stature
  • Hearing impairment
  • Microcephaly


SOURCES: MESH ORPHANET OMIM MENDELIAN

More info about THIAMINE-RESPONSIVE MEGALOBLASTIC ANEMIA SYNDROME

Top 5 symptoms//phenotypes associated to Lymphoma and Congestive heart failure

Symptoms // Phenotype % cases
Hearing impairment Common - Between 50% and 80% cases
Anemia Common - Between 50% and 80% cases
Leukemia Uncommon - Between 30% and 50% cases
Headache Uncommon - Between 30% and 50% cases
Ataxia Uncommon - Between 30% and 50% cases

Other less frequent symptoms

Patients with Lymphoma and Congestive heart failure. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases

Neutropenia Seizures Diarrhea Thrombocytopenia Neoplasm Fever Failure to thrive Short stature Splenomegaly Hepatomegaly Renal insufficiency Intellectual disability Growth delay Cardiomyopathy Global developmental delay Abnormal cardiac septum morphology Atrial septal defect Nystagmus Abnormality of the kidney Pancytopenia Abnormal heart morphology Hydrocephalus Ventriculomegaly Cryptorchidism Strabismus Hypertelorism Weight loss Vomiting Proptosis Stroke Multiple cafe-au-lait spots Malabsorption Polyneuropathy Migraine Premature birth Abnormality of skin pigmentation Astigmatism Scoliosis Hypothyroidism Autoimmunity Arrhythmia Diabetes mellitus Immunodeficiency Recurrent infections Pneumonia Respiratory tract infection Arthritis B-cell lymphoma Combined immunodeficiency

Rare Symptoms - Less than 30% cases

Multiple lentigines Intrauterine growth retardation Myopia Subvalvular aortic stenosis Cafe-au-lait spot Depressed nasal bridge Abnormal facial shape Multifocal epileptiform discharges Sensorineural hearing impairment Open mouth Hemiparesis Lymphoproliferative disorder Cardiomegaly Paresthesia Thick upper lip vermilion Hepatosplenomegaly Pleural effusion Cranial nerve paralysis Vasculitis Anorexia Short neck Dementia Abnormality of the dentition Abnormality of vision Azoospermia Hydroureter Bone marrow hypocellularity Malnutrition Melanocytic nevus Fine hair Abnormality of the ulna Myelodysplasia Abnormality of the testis Gliosis Kyphosis Nephropathy Bulbous nose Recurrent upper respiratory tract infections Hip dislocation Abnormal aortic valve morphology Scarring Umbilical hernia Osteopenia Bronchiectasis Bilateral sensorineural hearing impairment Bruising susceptibility Generalized hypotonia Carcinoma Ptosis High palate Retinal dystrophy Visual impairment Verrucae Epicanthus Long face Villous atrophy Peripheral axonal neuropathy Frontal bossing Abnormality of the liver Constipation Abnormality of cardiovascular system morphology Dolichocephaly Irritability Abnormality of the eye Purpura Respiratory failure Type I diabetes mellitus Polyhydramnios Abnormal lung morphology High forehead Inflammatory abnormality of the skin Gastroesophageal reflux Clinodactyly of the 5th finger Lymphadenopathy Hypertrophic cardiomyopathy Cataract Reduced bone mineral density Visual loss Ventricular septal defect Recurrent urinary tract infections Otitis media Macrocephaly Micrognathia Optic atrophy Fatigue Feeding difficulties Microcephaly Peripheral neuropathy Pallor Decreased antibody level in blood Vertigo Dysarthria Muscular hypotonia Abnormal hair pattern Long palpebral fissure Abnormality of the sternum Abnormal eyelash morphology Infantile spasms Dystrophic fingernails Neurofibromas Neurodevelopmental delay Aplasia/Hypoplasia of the eyebrow Open bite Large for gestational age Abnormality of the optic nerve Curly hair Abnormal heart valve morphology Underdeveloped supraorbital ridges Arnold-Chiari type I malformation Delayed CNS myelination Enlarged kidney Absent eyelashes Atopic dermatitis Hypoplasia of the zygomatic bone Premature skin wrinkling Abnormal myocardium morphology Anal stenosis Absent eyebrow Abnormality of the gastrointestinal tract Submucous cleft hard palate Short attention span Woolly hair Abnormality of refraction Generalized hyperpigmentation Alopecia of scalp Biparietal narrowing Poor appetite Sleep apnea Obsessive-compulsive behavior Thick vermilion border Progressive visual loss Growth hormone deficiency Webbed neck Dental malocclusion Intestinal malrotation Vesicoureteral reflux Nevus Full cheeks Abnormal bleeding Abdominal distention Palmoplantar keratoderma Sleep disturbance High, narrow palate Hepatic steatosis Falls Narrow forehead Nail dystrophy Feeding difficulties in infancy Erythema Sparse hair Pectus carinatum Neurological speech impairment Pruritus Abnormality of the cerebral white matter Joint hypermobility Hypermetropia Hypotrichosis Pulmonic stenosis Genu valgum Dry skin Ichthyosis Abnormality of the cardiovascular system Coarctation of aorta Heart murmur Brittle hair Palmoplantar hyperkeratosis Relative macrocephaly Poor suck Hyperextensible skin Deep philtrum Redundant skin Failure to thrive in infancy Delayed gross motor development Bilateral ptosis Sparse eyebrow Scaling skin Ectropion Cubitus valgus Chronic otitis media Optic nerve hypoplasia Abnormality of the genitourinary system Low posterior hairline Aspiration Myocardial infarction Decreased body weight Thickened skin Lymphedema Hyperpigmentation of the skin Cerebral visual impairment Abnormality of the nail Hemangioma Narrow palate Sparse eyelashes Oculomotor apraxia Cutis laxa Abnormal palate morphology Aplasia/Hypoplasia of the corpus callosum Deep palmar crease Anterior creases of earlobe Gastrointestinal dysmotility Tremor Aminoaciduria Cone/cone-rod dystrophy Polycystic ovaries Abnormal autonomic nervous system physiology Hallucinations Peripheral demyelination Neuronal loss in central nervous system Hypotension Urinary incontinence Coma Paraplegia Facial palsy Hyporeflexia Areflexia Spasticity Cardiac arrest Astrocytosis Diabetes insipidus Decreased muscle mass Megalencephaly Megaloblastic anemia Facial hypotonia Large forehead Macrocytic anemia Pain Secondary amenorrhea Hyperglycemia Minimal subcutaneous fat Hyperplasia of midface Hypovolemic shock Muscle weakness Hoarse voice Situs inversus totalis Focal impaired awareness seizure Urinary retention Multiple myeloma Stroke-like episode Constrictive median neuropathy Myelopathy Abnormal renal physiology Sensory ataxia Psychomotor deterioration Increased CSF protein Orthostatic hypotension due to autonomic dysfunction Vitreous floaters Cardiac amyloidosis Amyloid deposition in the vitreous humor Hypoglycemia Lethargy Restrictive cardiomyopathy Syringomyelia Amenorrhea Cachexia Abnormality of the skin Paraparesis Aciduria Retinal degeneration Spastic paraparesis Atrioventricular block Rheumatoid arthritis Amyloidosis Cerebral hemorrhage Impotence Aphasia Axonal degeneration Orthostatic hypotension Decreased number of peripheral myelinated nerve fibers Abdominal situs inversus Tented upper lip vermilion Abnormal mitral valve morphology Hypoplasia of the frontal lobes Eyelid fasciculation Multiple palmar creases Abnormality of the auditory canal Inappropriate crying Cutaneous T-cell lymphoma Morphological abnormality of the gastrointestinal tract Puberty and gonadal disorders Abnormal location of ears Abnormality of the hairline Hyperkeratosis pilaris Tongue thrusting Functional abnormality of the gastrointestinal tract Laryngeal cleft Generalized ichthyosis Optic nerve dysplasia Oral aversion Cavernous hemangioma Slow-growing hair Thickened helices Hyperextensibility of the finger joints Abnormality of the pulmonary artery Excessive wrinkled skin Abnormality of hair texture Paroxysmal atrial tachycardia Patchy alopecia Sparse or absent eyelashes Increased nuchal translucency Endocarditis Frontal balding Abnormality of the optic disc Abnormal tricuspid valve morphology Multiple plantar creases Telecanthus Drooling Status epilepticus Joint laxity Wide mouth Severe global developmental delay Inability to walk Highly arched eyebrow Focal-onset seizure Thick lower lip vermilion Absent speech Sideroblastic anemia Narrow face Increased body weight Abnormality of the basal ganglia Nephrocalcinosis Shock Difficulty walking Wide nasal bridge Progressive peripheral neuropathy Gout Jaundice Cirrhosis Hyperbilirubinemia Cholelithiasis Prolonged neonatal jaundice Reticulocytosis Anemia of inadequate production Reduced activity of N-acetylglucosaminyltransferase II Chronic myelogenous leukemia Congenital hypoplastic anemia Increased total bilirubin Increased hemoglobin Increased red cell osmotic fragility Endopolyploidy on chromosome studies of bone marrow Low-set, posteriorly rotated ears Abnormal aortic morphology Aggressive behavior Abnormal cerebellum morphology Atherosclerosis Opacification of the corneal stroma Lymphopenia Abnormality of epiphysis morphology Heterotopia Abnormal form of the vertebral bodies Intellectual disability, profound Lumbar hyperlordosis Nephrotic syndrome Microdontia Decreased testicular size Waddling gait Brain atrophy Stage 5 chronic kidney disease Coarse hair Platyspondyly Corneal opacity Hyperlordosis Developmental regression Proteinuria Thin upper lip vermilion Cerebellar atrophy Hypertension Motor delay Cognitive impairment Polyclonal elevation of IgM Cryoglobulinemia Impaired lymphocyte transformation with phytohemagglutinin Hyperlipidemia Chronic kidney disease Retinal hemorrhage Ovoid vertebral bodies Encephalomalacia Increased thyroid-stimulating hormone level Shallow acetabular fossae Steroid-resistant nephrotic syndrome Mucopolysacchariduria Hypoplasia of the capital femoral epiphysis Arteriosclerosis Right ventricular cardiomyopathy Cellular immunodeficiency Dentinogenesis imperfecta Precocious atherosclerosis Cerebral ischemia Disproportionate short-trunk short stature Thoracic kyphosis Encephalitis Transient ischemic attack Abnormality of the vasculature Protuberant abdomen Glomerulopathy Steatorrhea Hypermelanotic macule High pitched voice Emphysema Focal segmental glomerulosclerosis Spondyloepiphyseal dysplasia Nephritis Glomerulonephritis Epiphyseal dysplasia Glomerulosclerosis Monoclonal immunoglobulin M proteinemia Abnormality of neutrophils Abnormal immunoglobulin level Tonsillitis Interstitial pulmonary abnormality Inflammation of the large intestine Clubbing Abnormal intestine morphology Conjunctivitis Chronic diarrhea Recurrent otitis media Asthma Hemolytic anemia Recurrent respiratory infections Myelokathexis Bone marrow hypercellularity Hypersegmentation of neutrophil nuclei Septic arthritis Autoimmune hemolytic anemia Folliculitis Abnormality of bone marrow cell morphology Abnormality of female external genitalia Abnormality of female internal genitalia Atelectasis Periodontitis IgG deficiency Cellulitis Osteomyelitis Leukocytosis Recurrent bacterial infections Meningitis Sinusitis Carious teeth Colitis Recurrent sinusitis Normocytic anemia Gastrointestinal hemorrhage Periorbital edema Reduced consciousness/confusion Abnormality of the retinal vasculature Hypercoagulability Edema of the lower limbs Raynaud phenomenon Pulmonary infiltrates Gingival bleeding Elevated erythrocyte sedimentation rate Cutis marmorata Urticaria Epistaxis Memory impairment Respiratory insufficiency IgA deficiency Burkitt lymphoma Follicular hyperplasia Generalized lymphadenopathy Interstitial pneumonitis Gastritis IgM deficiency Immune dysregulation Cor pulmonale Brain neoplasm Clubbing of fingers Chronic lung disease Exocrine pancreatic insufficiency Autoimmune thrombocytopenia Fatigable weakness Abnormal T cell morphology Moyamoya phenomenon Hydronephrosis Partial duplication of thumb phalanx Aplasia/Hypoplasia of the uvula Neoplasm of head and neck Deficient excision of UV-induced pyrimidine dimers in DNA Anemic pallor Prolonged G2 phase of cell cycle Abnormal carotid artery morphology Almond-shaped palpebral fissure Compensated hypothyroidism Absent testis Hypoplastic anemia Chromosomal breakage induced by crosslinking agents Decreased fertility in males Clubbing of toes Complete duplication of thumb phalanx Pyridoxine-responsive sideroblastic anemia Aplasia/Hypoplasia of the iris Low-grade fever Meckel diverticulum Duplicated collecting system Duodenal stenosis Primary hypothyroidism Abnormality of nervous system morphology Reticulocytopenia Abnormality of chromosome stability Abnormal localization of kidney Abnormal renal morphology Abnormality of the hypothalamus-pituitary axis Acute monocytic leukemia Aplasia/Hypoplasia of fingers Abnormality of the preputium Bicornuate uterus Pectus excavatum EEG abnormality Coarse facial features Macrotia Autism Hyperkeratosis Cerebral cortical atrophy Hyperhidrosis Prominent forehead Posteriorly rotated ears Alopecia Delayed skeletal maturation Inguinal hernia Encephalopathy Depressivity Low-set ears Hernia Cerebral atrophy Malar flattening Long philtrum Short nose Behavioral abnormality Hypertonia Blindness Intellectual disability, severe Edema Anteverted nares Dysphagia Downslanted palpebral fissures Delayed speech and language development Abnormality of femur morphology Abnormality of the thumb Premature arteriosclerosis Small for gestational age Abnormality of the genital system Choanal atresia Short palpebral fissure Oligohydramnios Sloping forehead Tetralogy of Fallot Renal agenesis Hypopigmentation of the skin Anal atresia Facial asymmetry Abnormality of the foot Toe syndactyly Finger syndactyly Postnatal growth retardation Telangiectasia Pes planus Upslanted palpebral fissure Hypogonadism Severe short stature Patent ductus arteriosus Hypospadias Microphthalmia Respiratory distress Abnormality of the skeletal system Hyperreflexia Cleft palate Lateral displacement of the femoral head Nephrosclerosis Anterior pituitary dysgenesis Aganglionic megacolon Short thumb Abnormality of the uterus Absent thumb Aplastic anemia Abnormality of the upper limb Arteriovenous malformation Abnormal eyelid morphology Chromosome breakage Hearing abnormality External ear malformation Irregular hyperpigmentation Aplasia/Hypoplasia of the radius Absent radius Abnormality of blood and blood-forming tissues Acute myeloid leukemia Myeloid leukemia Ectopic kidney Insulin resistance Squamous cell carcinoma Hypoplasia of the ulna Glucose intolerance Tracheoesophageal fistula Triphalangeal thumb Hyperinsulinemia Abnormality of the urinary system Hypopigmented skin patches Renal hypoplasia/aplasia Leukopenia Horseshoe kidney Hypergonadotropic hypogonadism Spina bifida Abnormal vertebral morphology Thiamine-responsive megaloblastic anemia


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