Congestive heart failure, and Hodgkin lymphoma

Diseases related with Congestive heart failure and Hodgkin lymphoma

In the following list you will find some of the most common rare diseases related to Congestive heart failure and Hodgkin lymphoma 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

Low match COMBINED IMMUNODEFICIENCY DUE TO LRBA DEFICIENCY


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

Low 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:

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

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

Low match CARDIOFACIOCUTANEOUS SYNDROME


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

Low match CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE II


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

Low match DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 3; DKCA3


Dyskeratosis congenita is an inherited bone marrow failure syndrome classically characterized by the triad of mucosal leukoplakia, nail dysplasia, and abnormal skin pigmentation. Affected individuals have an increased risk of aplastic anemia and malignancy. Less common features include epiphora, premature gray hair, microcephaly, developmental delay, and pulmonary fibrosis, among others. The phenotype is highly variable. All affected individuals have shortened telomeres due to a defect in telomere maintenance (summary by Savage et al., 2008).For a discussion of genetic heterogeneity of dyskeratosis congenita, see DCKA1 (OMIM ).

Related symptoms:

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


SOURCES: OMIM MENDELIAN

More info about DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 3; DKCA3

Low match POLYHYDRAMNIOS-MEGALENCEPHALY-SYMPTOMATIC EPILEPSY SYNDROME


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

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 Congestive heart failure and Hodgkin lymphoma

Symptoms // Phenotype % cases
Hearing impairment Common - Between 50% and 80% cases
Anemia Common - Between 50% and 80% cases
Lymphoma Common - Between 50% and 80% cases
Leukemia Uncommon - Between 30% and 50% cases
Ataxia Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases


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

Rare Symptoms - Less than 30% cases


Abnormal facial shape Azoospermia Hydroureter Bronchiectasis Abnormality of the ulna Gliosis Aplastic anemia Nephropathy Bulbous nose Open mouth Abnormality of the testis Recurrent upper respiratory tract infections Hip dislocation Scarring Abnormal aortic valve morphology Multifocal epileptiform discharges Dementia Malnutrition Kyphosis Abnormality of the dentition Hyperpigmentation of the skin Short neck Myopia Hypertension Depressed nasal bridge Verrucae Reduced bone mineral density Abnormality of vision Melanocytic nevus Cataract Abnormal heart morphology Umbilical hernia Abnormality of cardiovascular system morphology Respiratory failure Carcinoma Hypertrophic cardiomyopathy Abnormality of the eye Frontal bossing Irritability Epicanthus Visual impairment High palate Ptosis Abnormality of the liver Arrhythmia Micrognathia Decreased antibody level in blood Otitis media Microcephaly Recurrent urinary tract infections Thick upper lip vermilion Dolichocephaly Hepatosplenomegaly Bruising susceptibility Multiple lentigines Subvalvular aortic stenosis Cafe-au-lait spot Leukopenia Cardiomegaly Hemiparesis Clinodactyly of the 5th finger Lymphoproliferative disorder Nail dystrophy Peripheral axonal neuropathy Dry skin Constipation Fatigue Gastrointestinal hemorrhage Generalized hypotonia Polyneuropathy Vertigo Cranial nerve paralysis Muscular hypotonia Villous atrophy Stroke Feeding difficulties Delayed speech and language development Dysarthria Macrocephaly Vasculitis Alopecia Interstitial pulmonary abnormality High forehead Polyhydramnios Peripheral neuropathy Long face Inflammatory abnormality of the skin Lymphadenopathy Type I diabetes mellitus Diabetes mellitus Purpura Abnormal intestine morphology Pleural effusion Infantile spasms Alopecia of scalp Abnormal eyelash morphology Abnormality of the sternum Arnold-Chiari type I malformation Atopic dermatitis Underdeveloped supraorbital ridges Poor appetite Ichthyosis Anal stenosis Long palpebral fissure Abnormal heart valve morphology Biparietal narrowing Submucous cleft hard palate Curly hair Generalized hyperpigmentation Enlarged kidney Woolly hair Absent eyelashes Abnormal hair pattern Abnormality of the optic nerve Aggressive behavior Dystrophic fingernails Telecanthus Low-set, posteriorly rotated ears Feeding difficulties in infancy Erythema Sparse hair Pectus carinatum Neurological speech impairment Genu valgum Pruritus Abnormality of the cerebral white matter Hypermetropia Hypotrichosis Joint hypermobility Pulmonic stenosis Short attention span Abnormality of the gastrointestinal tract Premature skin wrinkling Hypoplasia of the zygomatic bone Neurofibromas Obsessive-compulsive behavior Falls Aspiration Hemangioma Delayed CNS myelination Abnormal palate morphology Abnormal bleeding Full cheeks Cutis laxa Oculomotor apraxia Nevus Sparse eyelashes Narrow palate Vesicoureteral reflux Abnormality of the nail Intestinal malrotation Abnormality of the genitourinary system Dental malocclusion Cerebral visual impairment Webbed neck Lymphedema Thickened skin Decreased body weight Growth hormone deficiency Progressive visual loss Abnormality of the cardiovascular system Myocardial infarction Low posterior hairline Coarctation of aorta Sleep apnea Abdominal distention Neurodevelopmental delay Ectropion Retinal dystrophy Aplasia/Hypoplasia of the eyebrow Thick vermilion border Open bite Large for gestational age Absent eyebrow Narrow forehead Heart murmur Hepatic steatosis Chronic otitis media Cubitus valgus High, narrow palate Scaling skin Delayed gross motor development Sparse eyebrow Bilateral ptosis Failure to thrive in infancy Brittle hair Redundant skin Deep philtrum Hyperextensible skin Poor suck Sleep disturbance Relative macrocephaly Palmoplantar hyperkeratosis Palmoplantar keratoderma Optic nerve hypoplasia Aplasia/Hypoplasia of the corpus callosum Sparse or absent eyelashes Abnormal myocardium morphology Thick lower lip vermilion Restrictive cardiomyopathy Multiple myeloma Large forehead Facial hypotonia Megalencephaly Decreased muscle mass Diabetes insipidus Focal impaired awareness seizure Tented upper lip vermilion Drooling Shock Nephrocalcinosis Increased body weight Narrow face Status epilepticus Astrocytosis Constrictive median neuropathy Sensory ataxia Pulmonary hemorrhage Abnormal renal physiology Myelopathy Wide nasal bridge Absent speech Stroke-like episode Focal-onset seizure Difficulty walking Joint laxity Wide mouth Severe global developmental delay Inability to walk Highly arched eyebrow Increased CSF protein Syringomyelia Phimosis Abnormal autonomic nervous system physiology Urinary incontinence Hypotension Neuronal loss in central nervous system Peripheral demyelination Bilateral sensorineural hearing impairment Hallucinations Paraparesis Paresthesia Spastic paraparesis Atrioventricular block Cachexia Impotence Rheumatoid arthritis Cerebral hemorrhage Coma Paraplegia Amyloidosis Hypovolemic shock Minimal subcutaneous fat Decreased number of peripheral myelinated nerve fibers Orthostatic hypotension Hyperplasia of midface Axonal degeneration Aphasia Sensorineural hearing impairment Facial palsy Muscle weakness Pain Spasticity Tremor Areflexia Hyporeflexia Reticulated skin pigmentation Urinary retention Abnormality of refraction Abnormal tricuspid valve morphology 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 Hypoplasia of the frontal lobes Optic nerve dysplasia Patchy alopecia Abnormality of the optic disc EEG abnormality Cardiac amyloidosis Deep palmar crease Gastrointestinal dysmotility Abnormal mitral valve morphology Slow-growing hair Thickened helices Hyperextensibility of the finger joints Abnormality of the pulmonary artery Anterior creases of earlobe Excessive wrinkled skin Abnormality of hair texture Cavernous hemangioma Increased nuchal translucency Endocarditis Frontal balding Abnormality of the auditory canal Multiple palmar creases Esophageal stricture Orthostatic hypotension due to autonomic dysfunction Cerebellar hypoplasia Osteoporosis Retinopathy Nail dysplasia Cerebral calcification Portal hypertension Epiphora Reduced activity of N-acetylglucosaminyltransferase II Pulmonary fibrosis Psychomotor deterioration Premature graying of hair Aseptic necrosis Oral leukoplakia Vitreous floaters Endopolyploidy on chromosome studies of bone marrow Eyelid fasciculation Prolonged neonatal jaundice Multiple plantar creases Oral aversion Jaundice Cirrhosis Hyperbilirubinemia Cholelithiasis Reticulocytosis Increased red cell osmotic fragility Gout Anemia of inadequate production Chronic myelogenous leukemia Congenital hypoplastic anemia Increased total bilirubin Increased hemoglobin Hydronephrosis Abnormal localization of kidney Coarse facial features 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 Motor delay Cognitive impairment Polyclonal elevation of IgM Cryoglobulinemia Impaired lymphocyte transformation with phytohemagglutinin Monoclonal immunoglobulin M proteinemia Hyperlipidemia Chronic kidney disease Abnormality of neutrophils Thoracic kyphosis 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 Ovoid vertebral bodies Transient ischemic attack Encephalitis Abnormality of the vasculature Protuberant abdomen Glomerulopathy Steatorrhea Hypermelanotic macule High pitched voice Emphysema Focal segmental glomerulosclerosis Spondyloepiphyseal dysplasia Nephritis Glomerulonephritis Epiphyseal dysplasia Glomerulosclerosis Retinal hemorrhage Normocytic anemia Abnormal T cell morphology Septic arthritis Colitis Inflammation of the large intestine Clubbing Conjunctivitis Chronic diarrhea Recurrent otitis media Asthma Hemolytic anemia Recurrent respiratory infections Myelokathexis Bone marrow hypercellularity Hypersegmentation of neutrophil nuclei Tonsillitis Folliculitis Recurrent sinusitis 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 Autoimmune hemolytic anemia IgA deficiency Periorbital edema Pallor 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 Anorexia Epistaxis Memory impairment Visual loss Fatigable weakness Respiratory insufficiency 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 Encephalomalacia Abnormal immunoglobulin level Macrotia Complete duplication of thumb phalanx 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 Partial duplication of thumb phalanx Aplasia/Hypoplasia of the iris Aplasia/Hypoplasia of fingers Low-grade fever Meckel diverticulum Duplicated collecting system Duodenal stenosis Primary hypothyroidism Abnormality of nervous system morphology Abnormal aortic morphology Reticulocytopenia Abnormality of chromosome stability Abnormal renal morphology Abnormality of the hypothalamus-pituitary axis Acute monocytic leukemia Abnormality of femur morphology Aplasia/Hypoplasia of the uvula Pyridoxine-responsive sideroblastic anemia Abnormality of the thumb Cerebral atrophy Gastroesophageal reflux Autism Hyperkeratosis Cerebral cortical atrophy Hyperhidrosis Prominent forehead Posteriorly rotated ears Delayed skeletal maturation Inguinal hernia Encephalopathy Pectus excavatum Depressivity Hernia Malar flattening Abnormality of the preputium Long philtrum Short nose Behavioral abnormality Hypertonia Blindness Intellectual disability, severe Edema Anteverted nares Ventricular septal defect Dysphagia Downslanted palpebral fissures Optic atrophy Low-set ears Bicornuate uterus Abnormality of the uterus Moyamoya phenomenon Pes planus 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 Small for gestational age Postnatal growth retardation Upslanted palpebral fissure Abnormality of the genital system 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 Premature arteriosclerosis Choanal atresia Aganglionic megacolon Abnormality of the upper limb Squamous cell carcinoma 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 Absent thumb Ectopic kidney Hypoplasia of the ulna Telangiectasia Glucose intolerance Tracheoesophageal fistula Triphalangeal thumb Myelodysplasia Hyperinsulinemia Abnormality of the urinary system Hypopigmented skin patches Renal hypoplasia/aplasia Horseshoe kidney Hypergonadotropic hypogonadism Spina bifida Abnormal vertebral morphology Insulin resistance Short thumb Amyloid deposition in the vitreous humor



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