Congestive heart failure, and Weight loss

Diseases related with Congestive heart failure and Weight loss

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


Top matches:

Medium match CONGENITAL MUSCULAR DYSTROPHY DUE TO LMNA MUTATION


Congenital muscular dystrophy due to LMNA mutation is a rare congenital muscular dystrophy characterized by prominent axial hypotonia, dropped head syndrome, predominantly proximal muscle weakness in upper limbs/distal in lower limbs (with absent, poor or lost motor development), joint contractures (initially distal, later proximal), spine rigidity, and early respiratory insufficiency, in the presence of moderately elevated serum creatine kinase. Cardiac arrhythmias and sudden death have been also reported.

CONGENITAL MUSCULAR DYSTROPHY DUE TO LMNA MUTATION Is also known as mdcl|lmna-related congenital muscular dystrophy|l-cmd

Related symptoms:

  • Global developmental delay
  • Generalized hypotonia
  • Growth delay
  • Failure to thrive
  • Muscle weakness


SOURCES: ORPHANET OMIM MESH MENDELIAN

More info about CONGENITAL MUSCULAR DYSTROPHY DUE TO LMNA MUTATION

Medium match THYROTOXIC PERIODIC PARALYSIS


Thyrotoxic periodic paralysis (TPP) is a rare neurological disease characterized by recurrent episodes of paralysis and hypokalemia during a thyrotoxic state.

THYROTOXIC PERIODIC PARALYSIS Is also known as thyrotoxic hypokalemic periodic paralysis

Related symptoms:

  • Muscle weakness
  • Hypertension
  • Hyperreflexia
  • Tremor
  • Obesity


SOURCES: OMIM ORPHANET MENDELIAN

More info about THYROTOXIC PERIODIC PARALYSIS

Medium match DIFFUSE CUTANEOUS SYSTEMIC SCLEROSIS


Diffuse cutaneous systemic sclerosis (dcSSc) is a subtype of Systemic Sclerosis (SSc; see this term) characterized by truncal and acral skin fibrosis with an early and significant incidence of diffuse involvement (interstitial lung disease, oliguric renal failure, diffuse gastrointestinal disease, and myocardial involvement).

DIFFUSE CUTANEOUS SYSTEMIC SCLEROSIS Is also known as progressive cutaneous systemic scleroderma|diffuse cutaneous systemic scleroderma|progressive cutaneous systemic sclerosis

Related symptoms:

  • Muscle weakness
  • Pain
  • Flexion contracture
  • Hypertension
  • Dysphagia


SOURCES: ORPHANET MENDELIAN

More info about DIFFUSE CUTANEOUS SYSTEMIC SCLEROSIS

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Other less relevant matches:

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 CARNEY COMPLEX, TYPE 1; CNC1


Carney complex is an autosomal dominant multiple neoplasia syndrome characterized by cardiac, endocrine, cutaneous, and neural myxomatous tumors, as well as a variety of pigmented lesions of the skin and mucosae. Carney complex may simultaneously involve multiple endocrine glands, similar to classic MEN syndromes (MEN1; {131100} and MEN2; {171400}). Carney complex shows some similarities to McCune-Albright syndrome (MAS ), a sporadic condition that is also characterized by multiple endocrine and nonendocrine tumors, and shares skin abnormalities and some nonendocrine tumors with the lentiginoses and certain of the hamartomatoses, particularly Peutz-Jeghers syndrome (PJS ). Carney complex is often associated with the unusual large-cell calcifying Sertoli cell tumor and psammomatous melanotic schwannomas (Kirschner et al., 2000; Stratakis et al., 2001).

CARNEY COMPLEX, TYPE 1; CNC1 Is also known as lamb syndrome|myxoma, spotty pigmentation, and endocrine overactivity|carney myxoma-endocrine complex|car|carney syndrome|name syndrome

Related symptoms:

  • Neoplasm
  • Muscle weakness
  • Pain
  • Hypertension
  • Fever


SOURCES: OMIM MENDELIAN

More info about CARNEY COMPLEX, TYPE 1; CNC1

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 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 PRIMARY SCLEROSING CHOLANGITIS


Primary sclerosing cholangitis (PSC) is a rare, slowly progressive liver disease characterized by inflammation and destruction of the intra- and/or extra-hepatic bile ducts that lead to cholestasis, liver fibrosis, liver cirrhosis and ultimately liver failure.

PRIMARY SCLEROSING CHOLANGITIS Is also known as psc

Related symptoms:

  • Pain
  • Hypertension
  • Hepatomegaly
  • Fever
  • Fatigue


SOURCES: ORPHANET OMIM MENDELIAN

More info about PRIMARY SCLEROSING CHOLANGITIS

Top 5 symptoms//phenotypes associated to Congestive heart failure and Weight loss

Symptoms // Phenotype % cases
Hypertension Common - Between 50% and 80% cases
Fatigue Uncommon - Between 30% and 50% cases
Muscle weakness Uncommon - Between 30% and 50% cases
Palpitations Uncommon - Between 30% and 50% cases
Tremor Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases


Pallor Pain Constipation Seizures Hyporeflexia Cerebral hemorrhage Paraganglioma Cachexia Osteoporosis Hyperhidrosis Renal insufficiency Fever Vomiting

Rare Symptoms - Less than 30% cases


Proteinuria Aniridia Glomerulosclerosis Hypercalcemia Dysphonia Diarrhea Spasticity Chest pain Hematuria Nausea Autoimmunity Malabsorption Conductive hearing impairment Growth hormone excess Impotence Episodic abdominal pain Hypotension Hearing impairment Osteopenia Dyspnea Heart murmur Arthritis Abnormality of the skin Nausea and vomiting Gynecomastia Hepatosplenomegaly Hepatomegaly Extraadrenal pheochromocytoma Pheochromocytoma Cardiomegaly Splenomegaly Hemangioma Cafe-au-lait spot Carcinoma Neoplasm Paroxysmal vertigo Positive regitine blocking test Elevated urinary norepinephrine Elevated urinary dopamine Paraganglioma of head and neck Elevated urinary epinephrine Episodic hyperhidrosis Respiratory distress Hypertension associated with pheochromocytoma Panic attack Hypertensive retinopathy Episodic paroxysmal anxiety Pulsatile tinnitus Adrenal pheochromocytoma Recurrent paroxysmal headache Cranial nerve compression Sinus tachycardia Amyloidosis Flushing Hydrocephalus Vocal cord paralysis Global developmental delay Headache Goiter Tachycardia Hyperthyroidism Thyroiditis Flexion contracture Periodic hypokalemic paresis Urinary retention Arrhythmia EMG abnormality Hypokalemia Generalized amyotrophy Celiac disease Aortic valve stenosis Uveitis Constrictive median neuropathy Hepatocellular carcinoma Acute hepatic failure Ulcerative colitis Inflammation of the large intestine Cholestatic liver disease Cholangitis Decreased body weight Prolonged prothrombin time Histiocytosis Abnormality of the thyroid gland Hypoalbuminemia Pleural effusion Cirrhosis Abnormal EKG Abnormal heart valve morphology Exertional dyspnea Aortic regurgitation Oculomotor apraxia Opacification of the corneal stroma Ascites Portal hypertension Hepatitis Cholestasis Hepatic fibrosis Type I diabetes mellitus Horizontal nystagmus Pancreatitis Cholelithiasis Vitamin D deficiency Vitamin E deficiency Abnormal eosinophil morphology Thyroid follicular hyperplasia Neoplasm of the gallbladder Strabismus Recurrent systemic pyogenic infections Short stature Cutaneous myxoma Myxoid subcutaneous tumors Dilated superficial abdominal veins Profuse pigmented skin lesions Hypertonia Cardiac myxoma Uterine leiomyoma Follicular thyroid carcinoma Follicular hyperplasia Testicular neoplasm Pituitary prolactin cell adenoma Fibroma Multiple lentigines Abnormal large intestine physiology Spider hemangioma Sclerosing cholangitis Chronic hepatic failure Communicating hydrocephalus Mitral regurgitation Cholangiocarcinoma Vitamin A deficiency Ventricular hypertrophy Pancytopenia Vitamin K deficiency Dry skin Pes cavus Abnormal biliary tract morphology Ophthalmoplegia Generalized tonic-clonic seizures Corneal opacity Palmar telangiectasia Elevated alkaline phosphatase of hepatic origin Polyclonal elevation of IgM Brachycephaly Mitral stenosis Abnormal mitral valve morphology Supranuclear gaze palsy Neuronal loss in central nervous system Paraparesis Abnormal autonomic nervous system physiology Vasculitis Hallucinations Hemiparesis Bilateral sensorineural hearing impairment Peripheral demyelination Migraine Amyloid deposition in the vitreous humor Urinary incontinence Gliosis Coma Polyneuropathy Nephropathy Peripheral axonal neuropathy Paresthesia Depressivity Cardiac amyloidosis Paraplegia Aphasia Multiple myeloma Restrictive cardiomyopathy Increased CSF protein Syringomyelia Decreased number of peripheral myelinated nerve fibers Orthostatic hypotension Axonal degeneration Myelopathy Spastic paraparesis Malnutrition Abnormal renal physiology Sensory ataxia Psychomotor deterioration Orthostatic hypotension due to autonomic dysfunction Rheumatoid arthritis Atrioventricular block Vitreous floaters Encephalopathy Abdominal pain Foam cells Supranuclear ophthalmoplegia Abnormality of toe Decreased beta-glucocerebrosidase protein and activity Bacterial endocarditis Calcification of the aorta Elevated serum acid phosphatase Abnormal aortic arch morphology Spontaneous, recurrent epistaxis Mitral valve calcification Slowed horizontal saccades Corneal crystals Abnormal saccadic eye movements Aortic valve calcification Reticular hyperpigmentation Abnormal aortic morphology Abnormality of the pulmonary artery Abnormal aortic valve morphology Stroke-like episode Cardiac valve calcification Hypometric horizontal saccades Facial palsy Peripheral neuropathy Schwannoma Dementia Jaundice Areflexia Cardiomyopathy Dysarthria Elevated hepatic transaminase Visual impairment Abnormal common carotid artery morphology Abnormality of the liver Sensorineural hearing impairment Nystagmus Ataxia Cardiovascular calcification Scarring Aortic arch calcification Pruritus Red hair Arachnoid hemangiomatosis Thyroid carcinoma Postprandial hyperglycemia Episodic flaccid weakness Respiratory paralysis Late-onset proximal muscle weakness Exercise-induced muscle fatigue Increased intramyocellular lipid droplets Shortened PR interval Impaired myocardial contractility Abnormality of muscle fibers Thyrotoxicosis with diffuse goiter Periodic paralysis Abnormality of peripheral nerve conduction Graves disease Heat intolerance Hypomagnesemia Hashimoto thyroiditis Rhabdomyolysis Prolonged QT interval Second degree atrioventricular block Episodic hypokalemia Hyperkalemia Skin ulcer Osteolytic defects of the phalanges of the hand Pulmonary infiltrates Xerostomia Scleroderma Telangiectasia of the skin Pulmonary fibrosis Osteolysis Telangiectasia Decreased urinary potassium Pulmonary arterial hypertension Carious teeth Arthralgia Gastroesophageal reflux Dysphagia Thyrotoxicosis with toxic multinodular goitre Thyrotoxicosis with toxic single thyroid nodule Transient hypophosphatemia Mildly elevated creatine phosphokinase Ventricular fibrillation Dyspareunia Myopathy Joint hyperflexibility Abnormality of the foot Limb muscle weakness Narrow chest Muscular dystrophy Hyperlordosis Elevated serum creatine phosphokinase Respiratory insufficiency Limitation of joint mobility Talipes equinovarus Gait disturbance Skeletal muscle atrophy Motor delay Feeding difficulties Muscular hypotonia Failure to thrive Growth delay Talipes Decreased fetal movement Myotonia Obesity Ophthalmoparesis Muscle stiffness Tetraplegia Muscle cramps Lower limb muscle weakness Paralysis Proptosis Hyperreflexia Myocardial infarction Axial muscle weakness Limb-girdle muscle weakness Neck muscle weakness Spinal rigidity Congenital muscular dystrophy Poor head control Respiratory insufficiency due to muscle weakness Severe muscular hypotonia Oliguria Decreased urine output Generalized hypopigmentation Congenital cataract Myalgia Proximal muscle weakness Episodic hypertension Renal artery stenosis Albuminuria Neoplasm of the endocrine system Raynaud phenomenon Retinopathy Stroke Generalized hypotonia Retinal capillary hemangioma Elevated calcitonin Renal cell carcinoma Thyroid crisis Heteronymous hemianopia Abnormality of hair density Abnormal visual field test Abnormality of the eye Papule Fourth cranial nerve palsy Macule Pituitary adenoma Macroorchidism Blue irides Increased circulating cortisol level Bipolar affective disorder Striae distensae Freckling Neurofibromas Confusion Hypermelanotic macule Precocious puberty Sarcoma Ischemic stroke Increased body weight Tall stature Nevus Hirsutism Internal ophthalmoplegia Enlarged pituitary gland Hypertensive crisis Diplopia Prolactin excess Increased circulating gonadotropin level Pericardial effusion Easy fatigability Ventricular arrhythmia Cranial nerve paralysis Hypogonadotrophic hypogonadism Progressive visual loss Adrenocorticotropic hormone deficiency Vertigo Infertility Delayed puberty Hypogonadism Blindness Ptosis Abnormal bowel sounds Narrow foramen obturatorium Male hypogonadism Menstrual irregularities Cranial nerve VI palsy Central adrenal insufficiency Euthyroid hyperthyroxinemia Abnormality of the pituitary gland Erectile abnormalities Bitemporal hemianopia Decreased fertility in males Adrenocorticotropin deficient adrenal insufficiency Female hypogonadism Increased thyroid-stimulating hormone level Hemianopia Decreased circulating ACTH level Sudden loss of visual acuity Decreased female libido Decreased fertility in females Secondary growth hormone deficiency Oculomotor nerve palsy Abnormality of the menstrual cycle Supraventricular arrhythmia Adenocarcinoma of the large intestine



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