Congestive heart failure, and Anxiety

Diseases related with Congestive heart failure and Anxiety

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


Top matches:

Medium match FAMILIAL DYSKINESIA AND FACIAL MYOKYMIA


Familial dyskinesia and facial myokymia is a rare paroxysmal movement disorder, with childhood or adolescent onset, characterized by paroxysmal choreiform, dystonic, and myoclonic movements involving the limbs (mostly distal upper limbs), neck and/or face, which can progressively increase in both frequency and severity until they become nearly constant. Patients may also present with delayed motor milestones, perioral and periorbital dyskinesias, dysarthria, hypotonia, and weakness.

FAMILIAL DYSKINESIA AND FACIAL MYOKYMIA Is also known as fdfm

Related symptoms:

  • Intellectual disability
  • Generalized hypotonia
  • Motor delay
  • Hyperreflexia
  • Dysarthria


SOURCES: ORPHANET MESH OMIM MENDELIAN

More info about FAMILIAL DYSKINESIA AND FACIAL MYOKYMIA

Medium match WOLFF-PARKINSON-WHITE SYNDROME


A group of conditions in which HEART VENTRICLE activation by the atrial impulse is faster than the normal impulse conduction from the SINOATRIAL NODE. In these pre-excitation syndromes, atrial impulses often bypass the ATRIOVENTRICULAR NODE delay and travel via ACCESSORY CONDUCTING PATHWAYS connecting the atrium directly to the BUNDLE OF HIS.

WOLFF-PARKINSON-WHITE SYNDROME Is also known as wpw syndrome

Related symptoms:

  • Pain
  • Respiratory distress
  • Cardiomyopathy
  • Congestive heart failure
  • Arrhythmia


SOURCES: OMIM ORPHANET MENDELIAN

More info about WOLFF-PARKINSON-WHITE SYNDROME

Medium match PARAGANGLIOMAS 4; PGL4


PARAGANGLIOMAS 4; PGL4 Is also known as paraganglioma, familial malignant|pheochromocytoma, extraadrenal, and cervical paraganglioma|carotid body tumors and multiple extraadrenal pheochromocytomas|pheochromocytoma, familial extraadrenal|paragangliomas, hereditary extraadrenal

Related symptoms:

  • Neoplasm
  • Pain
  • Hypertension
  • Congestive heart failure
  • Headache


SOURCES: OMIM MENDELIAN

More info about PARAGANGLIOMAS 4; PGL4

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Other less relevant matches:

Medium match MCLEOD NEUROACANTHOCYTOSIS SYNDROME


McLeod neuroacanthocytosis syndrome (MLS) is a form of neuroacanthocytosis (see this term) and is characterized clinically by a Huntington's disease-like phenotype with an involuntary hyperkinetic movement disorder, psychiatric manifestations and cognitive alterations, and biochemically by absence of the Kx antigen and by weak expression of the Kell antigens.

MCLEOD NEUROACANTHOCYTOSIS SYNDROME Is also known as mls|x-linked mcleod syndrome

Related symptoms:

  • Seizures
  • Short stature
  • Muscle weakness
  • Cognitive impairment
  • Anemia


SOURCES: ORPHANET OMIM MENDELIAN

More info about MCLEOD NEUROACANTHOCYTOSIS SYNDROME

Medium match AUTOSOMAL DOMINANT HYPOCALCEMIA


Autosomal dominant hypocalcemia (AD hypocalcemia) is a disorder of calcium homeostasis characterized by variable degrees of hypocalcemia with abnormally low levels of parathyroid hormone (PTH) and persistant normal or elevated calciuria.

AUTOSOMAL DOMINANT HYPOCALCEMIA Is also known as ad hypocalcemia|hypocalcemia, familial|hypercalciuric hypocalcemia

Related symptoms:

  • Seizures
  • Short stature
  • Optic atrophy
  • Fatigue
  • Congestive heart failure


SOURCES: ORPHANET OMIM MENDELIAN

More info about AUTOSOMAL DOMINANT HYPOCALCEMIA

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 TUBEROUS SCLEROSIS COMPLEX


Tuberous sclerosis complex (TSC) is a neurocutaneous disorder characterized by multisystem hamartomas and associated with neuropsychiatric features.

TUBEROUS SCLEROSIS COMPLEX Is also known as tuberous sclerosis|bourneville syndrome

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Neoplasm
  • Cognitive impairment


SOURCES: OMIM ORPHANET MENDELIAN

More info about TUBEROUS SCLEROSIS COMPLEX

Medium match FABRY DISEASE


Fabry disease (FD) is a progressive, inherited, multisystemic lysosomal storage disease characterized by specific neurological, cutaneous, renal, cardiovascular, cochleo-vestibular and cerebrovascular manifestations.

FABRY DISEASE Is also known as ceramide trihexosidase deficiency|hereditary dystopic lipidosis|fd|alpha-galactosidase a deficiency|diffuse angiokeratoma|gla deficiency|angiokeratoma corporis diffusum|anderson-fabry disease

Related symptoms:

  • Seizures
  • Short stature
  • Hearing impairment
  • Sensorineural hearing impairment
  • Pain


SOURCES: ORPHANET OMIM MESH MENDELIAN

More info about FABRY DISEASE

Medium match MELAS


MELAS (Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke) syndrome is a rare progressive multisystemic disorder characterized by encephalomyopathy, lactic acidosis, and stroke-like episodes. Other features include endocrinopathy, heart disease, diabetes, hearing loss, and neurological and psychiatric manifestations.

MELAS Is also known as mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes|melas syndrome|mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes

Related symptoms:

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


SOURCES: ORPHANET OMIM MESH MENDELIAN

More info about MELAS

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

Symptoms // Phenotype % cases
Arrhythmia Common - Between 50% and 80% cases
Fatigue Uncommon - Between 30% and 50% cases
Seizures Uncommon - Between 30% and 50% cases
Palpitations Uncommon - Between 30% and 50% cases
Cardiomyopathy Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases


Dyspnea Short stature Pain Tachycardia Optic atrophy Depressivity Chest pain Atrial fibrillation Atrioventricular block Hyperhidrosis Behavioral abnormality Cognitive impairment Hypertension Nausea Paresthesia Tremor Proteinuria Headache Abdominal pain Muscle cramps Carcinoma Weight loss Renal cell carcinoma Paraganglioma Recurrent paroxysmal headache Pulsatile tinnitus Hypothyroidism Hematuria Renal insufficiency Hypertension associated with pheochromocytoma Glomerulosclerosis Extraadrenal pheochromocytoma Personality changes Paraganglioma of head and neck Left ventricular hypertrophy Generalized-onset seizure Neoplasm Anemia Peripheral neuropathy Respiratory insufficiency Adrenal pheochromocytoma Intellectual disability Episodic paroxysmal anxiety Cardiac arrest Dystonia Hypertonia Hypertrophic cardiomyopathy Stroke Vertigo Sudden cardiac death Dysarthria Hypotension Dilated cardiomyopathy Supraventricular tachycardia Involuntary movements Motor delay Wolff-Parkinson-White syndrome

Rare Symptoms - Less than 30% cases


Episodic hyperhidrosis Positive regitine blocking test Episodic abdominal pain Vocal cord paralysis Flushing Sinus tachycardia Elevated urinary dopamine Glomerulopathy Elevated urinary norepinephrine Panic attack Cranial nerve compression Aniridia Xerostomia Hypertensive retinopathy Transient ischemic attack Pallor Cerebral hemorrhage Hypoparathyroidism Dysesthesia EMG abnormality Increased intracranial pressure Reduced bone mineral density Hypercalciuria Basal ganglia calcification Reduced consciousness/confusion Renal tubular dysfunction Abnormal renal physiology Writer's cramp Conductive hearing impairment Congenital cataract Tubulointerstitial nephritis Dysphonia Hypercalcemia Paroxysmal vertigo Malabsorption Cafe-au-lait spot Cataract Abnormality of neuronal migration Nephrotic syndrome Emphysema Abnormality of the cardiovascular system Hearing impairment Sensorineural hearing impairment Nephropathy Fever Hypopigmented skin patches Delayed puberty Nausea and vomiting Vomiting Diarrhea Constipation Myalgia Developmental regression Ventricular hypertrophy Anorexia Global developmental delay Attention deficit hyperactivity disorder Progressive sensorineural hearing impairment Bundle branch block Pruritus Autism EEG abnormality Hemiplegia Abnormality of the liver Chronic kidney disease Exercise intolerance Papule Specific learning disability Cerebral calcification Subcutaneous nodule Easy fatigability Ischemic stroke Purpura Bradycardia Dilatation Elevated urinary epinephrine Abnormality of the renal tubule Elevated serum creatine phosphokinase Dyskinesia Rhabdomyolysis Chorea Emotional lability Ventricular arrhythmia Hallucinations Memory impairment Confusion Abnormality of the cerebral white matter Mental deterioration Dementia Areflexia Myoclonus Cerebral atrophy Myopathy Dysphagia Gait disturbance Hepatomegaly Muscle weakness Orofacial dyskinesia Respiratory distress Syncope Ventricular fibrillation Shortened PR interval Abnormality of movement Pheochromocytoma Hyperreflexia Impaired temperature sensation Angiokeratoma corporis diffusum Abnormal mitochondrial shape Cerebellar hypoplasia Supraventricular arrhythmia Delayed skeletal maturation Cochlear degeneration Conjunctival telangiectasia Hyporeflexia Visual loss Encephalopathy Kyphosis Cerebellar atrophy Abnormality of the dentition Progressive night blindness Blindness Short neck Ventriculomegaly Paralytic ileus Skeletal muscle atrophy Microalbuminuria Primary hypothyroidism Biventricular hypertrophy Abnormal endocardium morphology Abnormality of cardiovascular system physiology Rod-cone dystrophy Hypogonadism Osteoporosis Feeding difficulties in infancy Lethargy Hemeralopia Abnormal macular morphology Generalized tonic-clonic seizures Spotty hypopigmentation Neurological speech impairment Nyctalopia Erythema Protruding ear Abnormality of the pinna Abnormal cornea morphology Apnea Feeding difficulties Photophobia Paronychia Jaundice Gastroesophageal reflux Acidosis Gait ataxia Abnormal mitochondrial morphology Edema of the dorsum of hands Cochlear malformation Cerebral cortical atrophy Diabetes mellitus Visual impairment Decreased female libido Shortened QT interval Abnormality of glycosphingolipid metabolism Heavy proteinuria Tenesmus Distal renal tubular acidosis Left ventricular septal hypertrophy Increased blood urea nitrogen Tortuosity of conjunctival vessels Reduced sperm motility Angiokeratoma Hyperkeratotic papule Abnormality of the forehead Obstructive lung disease Bilateral intracranial calcifications Impaired renal concentrating ability Functional abnormality of the gastrointestinal tract ST segment depression Unexplained fevers Mucosal telangiectasiae Concentric hypertrophic cardiomyopathy Coronary artery stenosis Hyposthenuria Morphological abnormality of the vestibule of the inner ear Morphological abnormality of the inner ear Decreased lacrimation Vascular tortuosity Acroparesthesia Ptosis Crohn's disease Vascular skin abnormality Retinal vascular tortuosity Muscular hypotonia Corneal crystals Failure to thrive Nystagmus Abnormal cochlea morphology Hypertelorism Homonymous hemianopia Abnormality of acid-base homeostasis Growth delay Episodic quadriplegia Decreased glomerular filtration rate Limb pain Abnormality of temperature regulation Microcephaly Cornea verticillata Abnormal glomerular filtration rate Nephrogenic diabetes insipidus Abnormality of the common coagulation pathway Increased glomerular filtration rate Increased carotid artery intimal medial thickness Abnormal ST segment Abnormal common carotid artery morphology Ataxia Abnormality of visual evoked potentials Abnormality of the cerebellar vermis Retinal pigment epithelial atrophy Increased CSF lactate Hemiplegia/hemiparesis Mask-like facies Bifid scrotum Aplasia/Hypoplasia of the cerebellum Cerebral ischemia Gait imbalance Anterior hypopituitarism Stroke-like episode Seborrheic dermatitis Left ventricular failure Speech apraxia Abnormality of peripheral nerve conduction Overlapping toe Proximal tubulopathy Ileus Hemianopia Intestinal obstruction Episodic vomiting Motor polyneuropathy Ophthalmoparesis Abnormal thrombosis Psychomotor deterioration Muscle fiber atrophy Persistence of primary teeth Hyponatremia Focal segmental glomerulosclerosis Visual hallucinations Aortic aneurysm Vertebral fusion Atopic dermatitis Drowsiness Distal arthrogryposis Neonatal hypoglycemia Vitiligo Pulmonary embolism Heart block Primary adrenal insufficiency Mitochondrial myopathy Abnormality of immune system physiology Thyroiditis Hyperthyroidism Multiple lipomas Adrenal insufficiency Prolonged QT interval Progressive external ophthalmoplegia Posterior subcapsular cataract Delusions Visual field defect Cardiorespiratory arrest Hyperkalemia Dysphasia Facial diplegia Vestibular dysfunction Aphasia Aortic dissection Abnormality of mitochondrial metabolism Bilateral ptosis Psychotic episodes Abnormal cerebellum morphology Psychosis Status epilepticus Pulmonary arterial hypertension Type II diabetes mellitus Bilateral sensorineural hearing impairment Pigmentary retinopathy Amenorrhea Hip dysplasia Increased serum lactate Migraine Sensory impairment Generalized myoclonic seizures Postural instability Hypertrichosis Coma Polyneuropathy Hirsutism Polymicrogyria Lactic acidosis Hashimoto thyroiditis Ichthyosis Dysmetria Anal atresia Carious teeth Ophthalmoplegia Arthrogryposis multiplex congenita Hemiparesis Decreased body weight Decreased nerve conduction velocity Ragged-red muscle fibers Cachexia Growth abnormality Hyperkinesis Leber optic atrophy Spontaneous hematomas Gastroparesis Amaurosis fugax Auditory hallucinations Goiter Schizophrenia Mutism Abnormal nerve conduction velocity Renal Fanconi syndrome Gingival overgrowth Tubulointerstitial abnormality Reduced tendon reflexes External ophthalmoplegia Pancreatitis Macular degeneration Type I diabetes mellitus Hypogonadotrophic hypogonadism Generalized hirsutism Truncal ataxia Clonus Cerebral visual impairment Abnormality of retinal pigmentation Peripheral axonal neuropathy Myocardial infarction Tubulointerstitial fibrosis Hypokalemia Hypermagnesiuria Laryngospasm Cortical myoclonus Hypocalcemic seizures Increased circulating renin level Abnormal pattern of respiration Tetany Hyperphosphatemia Hypomagnesemia Irregular hyperpigmentation Fatigable weakness Abnormality of the fingernails Retinal capillary hemangioma Nephrocalcinosis Hypocalcemia Abnormality of the nail Nephrolithiasis Eczema Dry skin Alopecia Abnormality of the astrocytes Hyporeflexia of upper limbs Abnormal facial expression Blood group antigen abnormality Recurrent singultus Elevated calcitonin Arachnoid hemangiomatosis Caudate atrophy Infantile spasms Gingival fibromatosis Astrocytoma Abnormality of the pancreas Abnormality of the respiratory system Skin tags Gingivitis Neoplasm of the pancreas Multiple renal cysts Nevus flammeus Hamartoma Multiple cafe-au-lait spots Macule Retinopathy Cortical dysplasia Prominent occiput Precocious puberty Aplasia/Hypoplasia of the corpus callosum Renal cyst Iris coloboma Episodic hypertension Renal artery stenosis Albuminuria Neoplasm of the endocrine system Raynaud phenomenon Hemangioma Abnormal corpus striatum morphology Abnormal lactate dehydrogenase activity Rhabdomyosarcoma Paroxysmal atrial fibrillation Splenomegaly Elevated urinary catecholamines Glomus jugular tumor Chemodectoma Gastrointestinal stroma tumor Neuroblastoma Cranial nerve paralysis Ventricular preexcitation with multiple accessory pathways Paroxysmal supraventricular tachycardia Ventricular preexcitation Prolonged QRS complex Atrial flutter Hepatosplenomegaly Muscle fibrillation Cardiomegaly Abnormal heart morphology Facial myokymia Paroxysmal dyskinesia Myokymia Limb hypertonia Resting tremor Delayed gross motor development Choreoathetosis Muscular hypotonia of the trunk Difficulty walking Babinski sign Rigidity Abnormal social behavior Insomnia Generalized limb muscle atrophy Personality disorder Increased muscle fatiguability Hyporeflexia of lower limbs Excessive salivation Tics Acanthocytosis Motor axonal neuropathy Left bundle branch block Ventricular extrasystoles Bipolar affective disorder Restlessness Elevated hepatic transaminase Impaired pain sensation Impaired vibration sensation in the lower limbs Bowel incontinence Sensory axonal neuropathy Obsessive-compulsive behavior Sleep apnea Sensorimotor neuropathy Neuronal loss in central nervous system Parkinsonism Sensory neuropathy Hemolytic anemia Lower limb muscle weakness Pneumothorax Abnormality of the pleura Chronic pain Coronary artery atherosclerosis Abnormality of lipid metabolism Aortic root aneurysm Wheezing Renal tubular acidosis Glycosuria Abnormal heart valve morphology Telangiectasia of the skin Celiac disease Orthostatic hypotension Interstitial pulmonary abnormality Elevated erythrocyte sedimentation rate Impotence Edema of the lower limbs Loss of consciousness Anhidrosis Polyuria Diabetes insipidus Tricuspid regurgitation Impaired vibratory sensation Clubbing Heart murmur Polydipsia Abnormality of the hand Prominent supraorbital ridges Tinnitus Abnormal EKG Elevated serum creatinine Progressive hearing impairment Abnormality of femur morphology Miosis T-wave inversion Abnormal aortic valve morphology Gastrointestinal dysmotility Periorbital fullness Abnormal mitral valve morphology Asymmetric septal hypertrophy High-frequency hearing impairment Abnormal myocardium morphology Restrictive cardiomyopathy Abnormality of the nose Chronic fatigue Tubular atrophy Myocardial fibrosis Sinus bradycardia Achalasia Chronic obstructive pulmonary disease Angina pectoris Clubbing of fingers Peripheral arterial stenosis Reduced ejection fraction Heat intolerance Large earlobe Oligospermia Abnormality of the gastrointestinal tract Corneal dystrophy Abnormal intestine morphology Chylothorax Hypomelanotic macule Posteriorly rotated ears Midface retrusion Edema Subependymal giant-cell astrocytoma Rhabdomyoma Subungual fibromas Achromatic retinal patches Pulmonary lymphangiomyomatosis Confetti-like hypopigmented macules Ungual fibroma Dental enamel pits Cardiac rhabdomyoma Mandibular prognathia Subependymal nodules Cortical tubers Chordoma Retinal hamartoma Angiofibromas Renal angiomyolipoma Optic nerve glioma Macrodactyly Shagreen patch Ependymoma Third degree atrioventricular block Adenoma sebaceum Hyperkeratosis Arthralgia Aortic regurgitation Mitral valve prolapse Ventricular tachycardia Hyperlipidemia Aminoaciduria Spontaneous abortion Abnormal autonomic nervous system physiology Fasciculations Lymphedema Hypohidrosis Abnormal lung morphology Mitral regurgitation Generalized hypotonia Thick lower lip vermilion Urinary incontinence Coarse facial features Abdominal distention Thick vermilion border Thick eyebrow Bulbous nose Stage 5 chronic kidney disease Corneal opacity Prominent nasal bridge Cough Skin rash Abnormality of the kidney Abnormality of the nervous system Arthritis Prominent ear helix



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