Congestive heart failure, and Pallor

Diseases related with Congestive heart failure and Pallor

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


Top matches:

Medium match HB BART'S HYDROPS FETALIS


Hb Bart's hydrops fetalis is the most severe form of alpha-thalassemia (see this term) and is almost always lethal. It is characterized by fetal onset of generalized edema, pleural and pericardial effusions, and severe hypochromic anemia.

HB BART'S HYDROPS FETALIS Is also known as alpha-thalassemia major|alpha-thalassemia hydrops fetalis|homozygous alpha0-thalassemia|hemoglobin bart's hydrops fetalis

Related symptoms:

  • Anemia
  • Hepatomegaly
  • Hydrocephalus
  • Congestive heart failure
  • Splenomegaly


SOURCES: ORPHANET MENDELIAN

More info about HB BART'S HYDROPS FETALIS

Medium match ACQUIRED IDIOPATHIC SIDEROBLASTIC ANEMIA


Acquired idiopathic sideroblastic anaemia is one of a group of disorders known as the myelodysplastic syndromes (MDS) characterised by ineffective haemopoiesis affecting one or more blood cell lineages (myeloid, erythroid or megakaryocytic) leading to peripheral blood cytopenias and an increased risk of developing leukaemia. Acquired idiopathic sideroblastic anaemia is now more commonly referred to as refractory anaemia with ringed sideroblasts or the acronym RARS.

ACQUIRED IDIOPATHIC SIDEROBLASTIC ANEMIA Is also known as rars|primary acquired sideroblastic anemia|refractory anemia with ringed sideroblasts|aisa

Related symptoms:

  • Pain
  • Anemia
  • Fatigue
  • Respiratory distress
  • Congestive heart failure


SOURCES: OMIM ORPHANET MENDELIAN

More info about ACQUIRED IDIOPATHIC SIDEROBLASTIC ANEMIA

Medium match CONGENITAL ATRANSFERRINEMIA


Congenital atransferrinemia is a very rare hematologic disease caused by a transferrin (TF) deficiency and characterized by microcytic, hypochromic anemia (manifesting with pallor, fatigue and growth retardation) and iron overload, and that can be fatal if left untreated.

CONGENITAL ATRANSFERRINEMIA Is also known as hypotransferrinemia, familial|congenital hypotransferrinemia

Related symptoms:

  • Growth delay
  • Anemia
  • Hepatomegaly
  • Fatigue
  • Congestive heart failure


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about CONGENITAL ATRANSFERRINEMIA

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Other less relevant matches:

Medium match TRIOSE PHOSPHATE-ISOMERASE DEFICIENCY


Triosephosphate isomerase (TPI) deficiency is a severe autosomal recessive inherited multisystem disorder of glycolytic metabolism characterized by hemolytic anemia and neurodegeneration.

Related symptoms:

  • Seizures
  • Global developmental delay
  • Generalized hypotonia
  • Muscle weakness
  • Muscular hypotonia


SOURCES: ORPHANET MESH OMIM MENDELIAN

More info about TRIOSE PHOSPHATE-ISOMERASE DEFICIENCY

Medium match TSH-SECRETING PITUITARY ADENOMA


A rare adenoma of the anterior lobe of the pituitary gland that produces thyrotropin. It is usually associated with goiter and hyperthyroidism.

TSH-SECRETING PITUITARY ADENOMA Is also known as thyrotroph adenoma|pituitary thyrotrophic adenoma|thyroid stimulating hormone-secreting pituitary adenoma|tsh-oma

Related symptoms:

  • Seizures
  • Ptosis
  • Hypertension
  • Tremor
  • Fatigue


SOURCES: ORPHANET MENDELIAN

More info about TSH-SECRETING PITUITARY ADENOMA

Medium match HEREDITARY PHEOCHROMOCYTOMA-PARAGANGLIOMA


Hereditary paraganglioma-pheochromocytomas (PGL/PCC) are rare neuroendocrine tumors represented by paragangliomas (occurring in any paraganglia from the skull base to the pelvic floor) and pheochromocytomas (adrenal medullary paragangliomas; see this term).

HEREDITARY PHEOCHROMOCYTOMA-PARAGANGLIOMA Is also known as familial pheochromocytoma-paraganglioma

Related symptoms:

  • Tremor
  • Fatigue
  • Congestive heart failure
  • Weight loss
  • Conductive hearing impairment


SOURCES: ORPHANET MENDELIAN

More info about HEREDITARY PHEOCHROMOCYTOMA-PARAGANGLIOMA

Medium match PHEOCHROMOCYTOMA


Pheochromocytomas are catecholamine-secreting tumors that usually arise within the adrenal medulla. Approximately 10% arise in extraadrenal sympathetic ganglia, and are referred to as 'paragangliomas.' Approximately 10% are malignant, and approximately 10% are hereditary (Maher and Eng, 2002; Dluhy, 2002).Bolande (1974) introduced the concept and designation of the neurocristopathies, and identified 'simple,' including pheochromocytoma and medullary carcinoma of the thyroid, and 'complex' neurocristopathies and neurocristopathic syndromes, including NF1 and MEN2.Knudson and Strong (1972) applied Knudson's 2-mutation theory to pheochromocytoma (see discussion in {180200}) and concluded that it fits.Maher and Eng (2002) reviewed the clinical entities and genes associated with pheochromocytoma.

PHEOCHROMOCYTOMA Is also known as pheochromocytoma, susceptibility to

Related symptoms:

  • Neoplasm
  • Hypertension
  • Tremor
  • Fatigue
  • Congestive heart failure


SOURCES: ORPHANET OMIM MENDELIAN

More info about PHEOCHROMOCYTOMA

Medium match GAUCHER DISEASE-OPHTHALMOPLEGIA-CARDIOVASCULAR CALCIFICATION SYNDROME


Gaucher disease - ophthalmoplegia - cardiovascular calcification is a variant of Gaucher disease, also known as a Gaucher-like disease that is characterized by cardiac involvement.

GAUCHER DISEASE-OPHTHALMOPLEGIA-CARDIOVASCULAR CALCIFICATION SYNDROME Is also known as cardiovascular gaucher disease|gaucher-like disease|gaucher disease type 3c

Related symptoms:

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


SOURCES: OMIM ORPHANET MENDELIAN

More info about GAUCHER DISEASE-OPHTHALMOPLEGIA-CARDIOVASCULAR CALCIFICATION SYNDROME

Medium match THIAMINE-RESPONSIVE MEGALOBLASTIC ANEMIA SYNDROME


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

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

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

Symptoms // Phenotype % cases
Fatigue Common - Between 50% and 80% cases
Anemia Common - Between 50% and 80% cases
Hepatomegaly Uncommon - Between 30% and 50% cases
Tremor Uncommon - Between 30% and 50% cases
Headache Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases


Seizures Weight loss Splenomegaly Palpitations Recurrent infections Hearing impairment Respiratory distress Global developmental delay Chest pain

Rare Symptoms - Less than 30% cases


Vocal cord paralysis Cerebral hemorrhage Paraganglioma Sinus tachycardia Episodic abdominal pain Aniridia Nausea Glomerulosclerosis Hypercalcemia Dysphonia Hematuria Recurrent paroxysmal headache Proteinuria Conductive hearing impairment Cranial nerve paralysis Vertigo Hyperhidrosis Hypertension Cranial nerve compression Panic attack Adrenal pheochromocytoma Paroxysmal vertigo Anorexia Polyneuropathy Stroke Visual loss Diarrhea Ataxia Pancytopenia Short stature Raynaud phenomenon Neoplasm Positive regitine blocking test Pulsatile tinnitus Elevated urinary norepinephrine Elevated urinary dopamine Paraganglioma of head and neck Elevated urinary epinephrine Extraadrenal pheochromocytoma Episodic hyperhidrosis Hypertension associated with pheochromocytoma Macrocytic anemia Hypertensive retinopathy Episodic paroxysmal anxiety Normocytic anemia Flushing Sideroblastic anemia Cardiomyopathy Arrhythmia Hypochromic anemia Spasticity Microcytic anemia Peripheral neuropathy Hepatosplenomegaly Oligohydramnios Hyporeflexia Tachycardia Hydrocephalus Decreased beta-glucocerebrosidase protein and activity Recurrent respiratory infections Bacterial endocarditis Calcification of the aorta Elevated serum acid phosphatase Spontaneous, recurrent epistaxis Supranuclear ophthalmoplegia Mitral valve calcification Abnormal aortic arch morphology Slowed horizontal saccades Abnormality of toe Cardiac valve calcification Abnormal saccadic eye movements Hypometric horizontal saccades Abnormal common carotid artery morphology Aortic arch calcification Cardiovascular calcification Microcephaly Preeclampsia Nystagmus Sensorineural hearing impairment Cryptorchidism Optic atrophy Ventricular septal defect Corneal crystals Abnormal aortic valve morphology Aortic valve calcification Oculomotor apraxia Brachycephaly Corneal opacity Generalized tonic-clonic seizures Ophthalmoplegia Dry skin Cardiomegaly Abnormal hemoglobin Ventricular hypertrophy Mitral regurgitation Decreased body weight Aortic valve stenosis Horizontal nystagmus Opacification of the corneal stroma Aortic regurgitation Reticular hyperpigmentation Cachexia Heart murmur Exertional dyspnea Abnormal heart valve morphology Abnormal EKG Mitral stenosis Communicating hydrocephalus Supranuclear gaze palsy Foam cells Abnormal mitral valve morphology Pericarditis Abnormality of the pulmonary artery Abnormal aortic morphology Atrial septal defect Hydrops fetalis Thrombocytopenia Cutis marmorata Autoimmunity Leukemia Malabsorption Lymphadenopathy Lymphoma Migraine Gastrointestinal hemorrhage Memory impairment Epistaxis Vasculitis Purpura Urticaria Pleural effusion Elevated erythrocyte sedimentation rate Renal insufficiency Gingival bleeding Pulmonary infiltrates Edema of the lower limbs Hypercoagulability Lymphoproliferative disorder Abnormality of the retinal vasculature Reduced consciousness/confusion Periorbital edema Abnormality of neutrophils Retinal hemorrhage Multifocal epileptiform discharges Monoclonal immunoglobulin M proteinemia Impaired lymphocyte transformation with phytohemagglutinin Cryoglobulinemia Proptosis Respiratory insufficiency Hypertonia Bilateral sensorineural hearing impairment Abnormal heart morphology Diabetes mellitus Gastroesophageal reflux Hypoglycemia Abnormal cardiac septum morphology Lethargy Paresthesia Retinal degeneration Retinal dystrophy Polyhydramnios Neutropenia Aciduria Abnormality of the skin Amenorrhea Situs inversus totalis Fever Cardiac arrest Hoarse voice Aminoaciduria Cone/cone-rod dystrophy Polycystic ovaries Myelodysplasia Hyperglycemia Secondary amenorrhea Megaloblastic anemia Abdominal situs inversus Abnormality of the basal ganglia Progressive peripheral neuropathy Paroxysmal atrial tachycardia Thiamine-responsive megaloblastic anemia Pes cavus Albuminuria Strabismus Myopathy Hypogonadism Kyphosis Osteopenia Nausea and vomiting Delayed puberty Infertility Dystonia Hypotension Progressive visual loss Diplopia Gynecomastia Hypogonadotrophic hypogonadism Ventricular arrhythmia Osteoporosis Goiter Easy fatigability Hypokalemia Impotence Pericardial effusion Hyperthyroidism Growth hormone excess Increased circulating gonadotropin level Prolactin excess Male hypogonadism Adrenocorticotropic hormone deficiency Menstrual irregularities Hemianopia Cerebral atrophy Vomiting Abnormality of the menstrual cycle Respiratory insufficiency due to muscle weakness Jaundice Hypertrophic cardiomyopathy Respiratory tract infection Abnormal pyramidal sign Limb muscle weakness Unsteady gait Hemolytic anemia Dyskinesia Neuronal loss in central nervous system Optic disc pallor Intention tremor Involuntary movements Progressive muscle weakness Decreased nerve conduction velocity Blindness Cholelithiasis Babinski sign Abnormality of immune system physiology Diaphragmatic paralysis Cholecystitis Nonspherocytic hemolytic anemia Normochromic anemia Abnormal posturing Chronic hemolytic anemia Congenital hemolytic anemia Central nervous system degeneration Ptosis Areflexia Supraventricular arrhythmia Oculomotor nerve palsy Pain Abnormal glucose tolerance Abnormality of the pancreas Abnormality of the cardiovascular system Cirrhosis Scarring Elevated calcitonin Abnormality of the liver Arthritis Hypothyroidism Pneumonia Growth delay Refractory sideroblastic anemia Crackles Retinal capillary hemangioma Decreased mean corpuscular volume Atransferrinemia Increased serum ferritin Arachnoid hemangiomatosis Irritability Carcinoma Retinopathy Congenital cataract Cafe-au-lait spot Hemangioma Neoplasm of the endocrine system Pheochromocytoma Respiratory failure Renal artery stenosis Episodic hypertension Hypochromic microcytic anemia Generalized hypotonia Secondary growth hormone deficiency Euthyroid hyperthyroxinemia Decreased fertility in females Decreased female libido Sudden loss of visual acuity Decreased circulating ACTH level Increased thyroid-stimulating hormone level Central adrenal insufficiency Female hypogonadism Adrenocorticotropin deficient adrenal insufficiency Decreased fertility in males Bitemporal hemianopia Erectile abnormalities Periodic hypokalemic paresis Abnormality of the pituitary gland Cranial nerve VI palsy Muscle weakness Enlarged pituitary gland Fourth cranial nerve palsy Internal ophthalmoplegia Abnormal visual field test Abnormality of hair density Heteronymous hemianopia Thyroid crisis Gait disturbance Skeletal muscle atrophy Hyperreflexia Motor delay Muscular hypotonia Renal cell carcinoma Polyclonal elevation of IgM



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