Congestive heart failure, and Erythema

Diseases related with Congestive heart failure and Erythema

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


Top matches:

Medium match NAXOS DISEASE


Naxos disease is a recessively inherited condition with arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) and a cutaneous phenotype, characterised by peculiar woolly hair and palmoplantar keratoderma.

NAXOS DISEASE Is also known as keratosis palmoplantaris with arrhythmogenic cardiomyopathy|palmoplantar hyperkeratosis with arrythmogenic cardiomyopathy|kwwh type i|keratoderma with woolly hair type i|mal de naxos|palmoplantar keratoderma with arrhythmogenic right ventricular cardiomyo

Related symptoms:

  • Fatigue
  • Cardiomyopathy
  • Congestive heart failure
  • Dilatation
  • Arrhythmia


SOURCES: MESH ORPHANET OMIM MENDELIAN

More info about NAXOS DISEASE

Medium match KAWASAKI DISEASE


Kawasaki disease (KD) is a febrile, systemic, self-limiting vasculitis affecting children and characterized by inflammation in the medium sized vessels associated with coronary arterial aneurysms (CAA) that may be life threatening when untreated. KD is the most common cause of acquired heart disease in children in developed countries and is a risk factor for ischemic heart disease in adulthood.

KAWASAKI DISEASE Is also known as kd|infantile polyarteritis|mucocutaneous lymph node syndrome

Related symptoms:

  • Sensorineural hearing impairment
  • Ptosis
  • Fever
  • Fatigue
  • Edema


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about KAWASAKI DISEASE

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Other less relevant matches:

Low match PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1


This autosomal recessive systemic autoinflammatory disorder is characterized by early childhood onset of annular erythematous plaques on the face and extremities with subsequent development of partial lipodystrophy and laboratory evidence of immune dysregulation. More variable features include recurrent fever, severe joint contractures, muscle weakness and atrophy, hepatosplenomegaly, basal ganglia calcifications, and microcytic anemia (summary by Agarwal et al., 2010; Kitamura et al., 2011; Arima et al., 2011).This disorder encompasses Nakajo-Nishimura syndrome (NKJO); joint contractures, muscular atrophy, microcytic anemia, and panniculitis-induced lipodystrophy (JMP syndrome); and chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature syndrome (CANDLE). Among Japanese patients, this disorder is best described as Nakajo-Nishimura syndrome, since both Nakajo (1939) and Nishimura et al. (1950) contributed to the original phenotypic descriptions. Genetic Heterogeneity of Proteasome-Associated Autoinflammatory SyndromeSee also PRAAS2 (OMIM ), caused by mutation in the POMP gene (OMIM ) on chromosome 13q12, and PRAAS3 (OMIM ), caused by mutation in the PSMB4 gene (OMIM ) on chromosome 1q21.

PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1 Is also known as chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature syndrome|candle|joint contractures, muscular atrophy, microcytic anemia, and panniculitis-induced lipodystrophy|autoinflammation, lipodystrophy, and dermatosis syndrome|n

Related symptoms:

  • Intellectual disability
  • Seizures
  • Short stature
  • Failure to thrive
  • Muscle weakness


SOURCES: OMIM ORPHANET MENDELIAN

More info about PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1

Low match INCONTINENTIA PIGMENTI


Incontinentia pigmenti (IP) is a rare X-linked dominant multi-systemic ectodermal dysplasia usually lethal in males and presenting neonatally in females with a bullous rash along Blashko's lines (BL) followed by verrucous plaques evolving over time to hyperpigmented swirling patterns. It is further characterized by teeth abnormalities, alopecia, nail dystrophy and affects occasionally the retina and the central nervous system (CNS).

INCONTINENTIA PIGMENTI Is also known as bloch-siemens syndrome|bloch-sulzberger syndrome

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Scoliosis


SOURCES: ORPHANET MENDELIAN

More info about INCONTINENTIA PIGMENTI

Low match SARCOIDOSIS


Sarcoidosis is a multisystemic disorder of unknown cause characterized by the formation of immune granulomas in involved organs.

SARCOIDOSIS Is also known as boeck sarcoid|besnier-boeck-schaumann disease|sarcoidosis|boeck's sarcoid

Related symptoms:

  • Seizures
  • Pain
  • Cataract
  • Anemia
  • Visual impairment


SOURCES: ORPHANET OMIM MENDELIAN

More info about SARCOIDOSIS

Low 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

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 VEIN OF GALEN ANEURYSMAL MALFORMATION


Vein of Galen aneurysmal malformation (VGAM) is a congenital vascular malformation characterized by dilation of the embryonic precursor of the vein of Galen. It is a sporadic lesion that occurs during embryogenesis.

VEIN OF GALEN ANEURYSMAL MALFORMATION Is also known as vein of galen arteriovenous malformations

Related symptoms:

  • Congestive heart failure
  • Headache
  • Dilatation
  • Abnormality of the cerebral vasculature
  • Prominent superficial veins


SOURCES: MESH ORPHANET MENDELIAN

More info about VEIN OF GALEN ANEURYSMAL MALFORMATION

Low match PARKES WEBER SYNDROME


Related symptoms:

  • Congestive heart failure
  • Headache
  • Glaucoma
  • Abnormal bleeding
  • Hemiparesis


SOURCES: ORPHANET MENDELIAN

More info about PARKES WEBER SYNDROME

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

Symptoms // Phenotype % cases
Arrhythmia Common - Between 50% and 80% cases
Seizures Uncommon - Between 30% and 50% cases
Headache Uncommon - Between 30% and 50% cases
Cardiomegaly Uncommon - Between 30% and 50% cases
Short stature Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases


Hepatomegaly Cataract Edema Fever Intellectual disability Hyperhidrosis Alopecia Fatigue Cardiomyopathy Pain Hyperkeratosis Dilatation Sudden cardiac death Arthritis Global developmental delay Lymphadenopathy Muscular hypotonia Skin rash Dilated cardiomyopathy Visual impairment Syncope Hyperpigmentation of the skin Cerebral cortical atrophy Pruritus Ichthyosis Nail dystrophy Ptosis Blindness Palpitations Palmoplantar keratoderma Dyspnea Skeletal muscle atrophy Elevated erythrocyte sedimentation rate Splenomegaly Thrombocytopenia Woolly hair Failure to thrive Tubulointerstitial nephritis Anemia Hemiparesis Ventricular tachycardia Scarring

Rare Symptoms - Less than 30% cases


Pulmonary arterial hypertension Abnormality of the nail Cerebral visual impairment Osteolysis Attention deficit hyperactivity disorder Eosinophilia Muscle weakness Abnormality of skin pigmentation Camptodactyly of finger Umbilical hernia Gait disturbance Growth abnormality Cognitive impairment Macrotia Osteopenia Strabismus Scoliosis Abnormality of the liver Hemiplegia/hemiparesis Erythema nodosum Immune dysregulation Basal ganglia calcification Increased antibody level in blood Abnormal bleeding Peripheral neuropathy Telangiectasia of the skin Delayed skeletal maturation Bilateral ptosis Vomiting Decreased body weight Abnormality of the dentition Hypertonia Kyphosis Cerebral atrophy Depressivity Encephalopathy Constipation Ventriculomegaly Autism Gastroesophageal reflux EEG abnormality Hypertrophic cardiomyopathy Feeding difficulties in infancy Neurological speech impairment Atopic dermatitis Peripheral axonal neuropathy Abnormality of the cardiovascular system Short neck Dysphagia Abnormality of immune system physiology Pleural effusion Uveitis Cerebral ischemia Respiratory distress Renal insufficiency Glaucoma Weight loss Hypothyroidism Photophobia Anorexia Hyperthyroidism Optic atrophy Heart block Abnormality of the gastrointestinal tract Hearing impairment Ataxia Growth delay Hypertelorism Nystagmus Feeding difficulties Dysarthria Hypercalciuria Hypopigmented skin patches Abnormal myocardium morphology Jaundice Ischemic stroke Conjunctivitis Absent eyebrow Decreased liver function Bundle branch block Myocardial infarction Right bundle branch block Aplasia/Hypoplasia of the eyebrow Migraine Nausea and vomiting Respiratory tract infection Irritability Proteinuria Arthralgia Hyponatremia Abdominal pain Diarrhea Sensorineural hearing impairment Peripheral arteriovenous fistula Right ventricular cardiomyopathy Abnormal heart morphology Abnormality of hair texture Vertigo Abnormal blistering of the skin Clubbing of fingers Alopecia of scalp Curly hair Brittle hair Scaling skin Cardiac arrest Chest pain Carious teeth Tachycardia Abnormal heart valve morphology Interstitial pulmonary abnormality Schizophrenia Gastroparesis Mutism Goiter Functional abnormality of the gastrointestinal tract Amaurosis fugax Spontaneous hematomas Tongue thrusting Hyperkeratosis pilaris Abnormality of the hairline Abnormal location of ears Hyperkinesis Leber optic atrophy Persistence of primary teeth Aphasia Puberty and gonadal disorders Writer's cramp Abnormal nerve conduction velocity Morphological abnormality of the gastrointestinal tract Muscle fiber atrophy Easy fatigability Cutaneous T-cell lymphoma Psychomotor deterioration Inappropriate crying Dysesthesia Motor polyneuropathy Chronic kidney disease Abnormality of the auditory canal Multiple palmar creases Episodic vomiting Eyelid fasciculation Auditory hallucinations Tubulointerstitial abnormality Renal Fanconi syndrome Neoplasm Episodic quadriplegia Bilateral intracranial calcifications Morphological abnormality of the vestibule of the inner ear Morphological abnormality of the inner ear Prominent ear helix Generalized hypotonia Micrognathia Homonymous hemianopia Cryptorchidism Low-set ears High palate Delayed speech and language development Depressed nasal bridge Epicanthus Abnormality of acid-base homeostasis Abnormal cochlea morphology Atrioventricular block Paronychia Psychotic episodes Abnormality of the cerebellar vermis Crohn's disease Hemeralopia Abnormal macular morphology Spotty hypopigmentation Abnormal mitochondrial morphology Ragged-red muscle fibers Edema of the dorsum of hands Cochlear malformation Progressive night blindness Cochlear degeneration Abnormal mitochondrial shape Paralytic ileus Multiple plantar creases Hemianopia Oral aversion Abnormality of neuronal migration Delusions Focal segmental glomerulosclerosis Transient ischemic attack Posterior subcapsular cataract Progressive external ophthalmoplegia Mitochondrial myopathy Hypoparathyroidism Xerostomia Vitiligo Vascular skin abnormality Neonatal hypoglycemia Abnormality of visual evoked potentials Hashimoto thyroiditis Varicose veins Drowsiness Facial diplegia Vertebral fusion Dysphasia Hyperkalemia Visual field defect Adrenal insufficiency Prolonged QT interval Multiple lipomas Progressive sensorineural hearing impairment Distal arthrogryposis Overlapping toe Glomerulopathy Rhabdomyolysis Thyroiditis Primary adrenal insufficiency Pulmonary embolism Cardiorespiratory arrest Mask-like facies Abnormality of the renal tubule Speech apraxia Decreased nerve conduction velocity Anterior hypopituitarism Stroke-like episode Cachexia Seborrheic dermatitis Left ventricular failure Retinal pigment epithelial atrophy Gait imbalance Abnormality of peripheral nerve conduction Prominent superficial veins Abnormality of the cerebral vasculature Proximal tubulopathy Ileus Vestibular dysfunction Increased head circumference Myopia Aortic dissection Wolff-Parkinson-White syndrome Renal tubular dysfunction Bifid scrotum Visual hallucinations Increased CSF lactate Aplasia/Hypoplasia of the cerebellum Intestinal obstruction Personality changes Hemiplegia Ophthalmoparesis Reduced consciousness/confusion Abnormality of mitochondrial metabolism Hypertrophy of the lower limb Aortic aneurysm Nevus flammeus Vein of Galen aneurysmal malformation Short nose Macrocephaly Optic nerve hypoplasia Aplasia/Hypoplasia of the corpus callosum Abnormal mitral valve morphology Hemangioma Sleep apnea Abnormality of the genitourinary system Delayed gross motor development Gastrointestinal dysmotility Cutis laxa Palmoplantar hyperkeratosis Abnormality of vision Relative macrocephaly Deep palmar crease Poor suck Hyperextensible skin Deep philtrum Abnormal palate morphology Slow-growing hair Failure to thrive in infancy Subvalvular aortic stenosis Progressive visual loss Narrow forehead Coarctation of aorta Low posterior hairline Fine hair Inflammatory abnormality of the skin Thickened helices Oculomotor apraxia Open mouth Thickened skin Cafe-au-lait spot Lymphedema Aspiration Narrow palate Sparse eyelashes Redundant skin Abnormality of refraction Webbed neck Submucous cleft hard palate Infantile spasms Abnormality of the sternum Long palpebral fissure Multiple cafe-au-lait spots Biparietal narrowing Generalized hyperpigmentation Anal stenosis Neurodevelopmental delay Underdeveloped supraorbital ridges Poor appetite Abnormal eyelash morphology Arnold-Chiari type I malformation Enlarged kidney Absent eyelashes Hypoplasia of the zygomatic bone Neurofibromas Hydroureter Sparse eyebrow Heart murmur Ectropion Delayed CNS myelination Melanocytic nevus Cubitus valgus Abnormality of the testis Chronic otitis media Abnormality of the optic nerve Dystrophic fingernails Malnutrition Abnormal hair pattern Thick upper lip vermilion Short attention span Abnormality of the ulna Obsessive-compulsive behavior Large for gestational age Open bite Growth hormone deficiency Abnormal aortic valve morphology Downslanted palpebral fissures Hydronephrosis Hypoplasia of the frontal lobes Proptosis Polyhydramnios Optic nerve dysplasia High forehead Coarse facial features Aggressive behavior Posteriorly rotated ears Telecanthus Low-set, posteriorly rotated ears Abnormality of the eye Abnormality of the kidney Sparse hair Abnormal cardiac septum morphology Pectus carinatum Prominent forehead Clinodactyly of the 5th finger Patchy alopecia Intellectual disability, severe Frontal bossing Ventricular septal defect Laryngeal cleft Anteverted nares Hydrocephalus Atrial septal defect Behavioral abnormality Inguinal hernia Generalized ichthyosis Premature skin wrinkling Long philtrum Malar flattening Abnormality of cardiovascular system morphology Hernia Pectus excavatum Leukemia Abnormal tricuspid valve morphology Dental malocclusion Excessive wrinkled skin Sparse or absent eyelashes High, narrow palate Multiple lentigines Sleep disturbance Abdominal distention Cavernous hemangioma External ophthalmoplegia Hepatic steatosis Full cheeks Abnormality of the pulmonary artery Nevus Vesicoureteral reflux Hyperextensibility of the finger joints Intestinal malrotation Premature birth Increased nuchal translucency Thick vermilion border Abnormality of the optic disc Genu valgum Anterior creases of earlobe Frontal balding Dolichocephaly Abnormality of the cerebral white matter Hypermetropia Hypotrichosis Pulmonic stenosis Astigmatism Retinal dystrophy Dry skin Long face Joint hypermobility Endocarditis Falls Bulbous nose Bruising susceptibility Reduced tendon reflexes Hypogonadism Pancreatitis Abnormally large globe Glucose intolerance Long fingers Hypermelanotic macule Microcytic anemia Rimmed vacuoles Myositis Generalized lipodystrophy Elbow flexion contracture Flexion contracture of toe Hypochromic anemia Panniculitis Episcleritis Stiff skin Finger swelling Lipodystrophy Lymphopenia Spasticity Recurrent infections Double outlet right ventricle with subpulmonary ventricular septal defect without pulmonary stenosis Strawberry tongue Aseptic leukocyturia Abnormal gallbladder morphology Flexion contracture Intellectual disability, mild Babinski sign Bone pain Hepatosplenomegaly Elevated hepatic transaminase Inability to walk Macroglossia Prominent nose Thick lower lip vermilion Hypertriglyceridemia Adipose tissue loss Microphthalmia Pyuria Absent hand Hypoplastic fingernail Verrucae Deviation of finger Supernumerary ribs Asymmetric growth Retinal hemorrhage Abnormal chorioretinal morphology Abnormal toenail morphology Ridged fingernail Abnormal hand morphology Broad nail Retinal vascular proliferation Proximal muscle weakness Facial palsy Cough Dystrophic toenail Hearing abnormality Finger syndactyly Skin ulcer Corneal opacity Oral cleft Retinal detachment Delayed eruption of teeth Hypodontia Blue sclerae Abnormality of the hair Irregular hyperpigmentation Abnormality of dental enamel Abnormality of the fingernails Spina bifida occulta Encephalitis Abnormality of dental morphology Keratitis Supernumerary nipple Abnormal emotion/affect behavior Arthralgia/arthritis Hepatic failure Akinesia Epidermal acanthosis Sparse scalp hair Long eyelashes Sparse and thin eyebrow Acanthosis nigricans Ventricular arrhythmia Exertional dyspnea Ectodermal dysplasia Fragile skin Ventricular extrasystoles Reduced ejection fraction Onycholysis Hypergranulosis T-wave inversion Cyanosis Sepsis Abnormal T-wave Abnormal EKG Oligodontia Reduced number of teeth Loss of consciousness Hypokinesia Agenesis of permanent teeth Parakeratosis Fragile nails Cleft upper lip Myocardial fibrosis Leukonychia Selective tooth agenesis Reduced systolic function Gingival recession Agenesis of molar Respiratory failure Acantholysis Prolonged QRS complex Abnormality of nail color Cholecystitis Recurrent pharyngitis Inflammatory abnormality of the eye Elevated C-reactive protein level Cheilitis Synovitis Ascending tubular aorta aneurysm Abnormal oral mucosa morphology Myocarditis Glossitis Arteritis Abnormal pericardium morphology Conjunctival hyperemia CSF pleocytosis Cervical lymphadenopathy Coronary artery aneurysm Allergy Aortic root aneurysm Right ventricular dilatation Mitral regurgitation Paroxysmal ventricular tachycardia Abnormal right ventricle morphology Ventricular flutter Abnormal morphology of right ventricular trabeculae Hematuria Hepatitis Cholestasis Acute kidney injury Meningitis Vasculitis Cranial nerve paralysis Hypoalbuminemia Leukocytosis Coronary artery atherosclerosis Pericarditis Papule Hemolytic anemia Macular degeneration Delayed puberty Generalized tonic-clonic seizures Lethargy Arthrogryposis multiplex congenita Ophthalmoplegia Congenital cataract Malabsorption Anal atresia Nyctalopia Dysmetria Paresthesia Confusion Lactic acidosis Nausea Polymicrogyria Stroke Protruding ear Nephropathy Osteoporosis Hyporeflexia Elevated serum creatine phosphokinase Cerebellar hypoplasia Rod-cone dystrophy Dementia Myoclonus Diabetes mellitus Abnormality of the pinna Gait ataxia Acidosis Myalgia Anxiety Apnea Mental deterioration Developmental regression Hirsutism Polyneuropathy Visual loss Hallucinations Atrial fibrillation Hypertrichosis Involuntary movements Left ventricular hypertrophy Gingival overgrowth Abnormality of retinal pigmentation Clonus Psychosis Truncal ataxia EMG abnormality Generalized hirsutism Hypogonadotrophic hypogonadism Type I diabetes mellitus Exercise intolerance Purpura Ventricular hypertrophy Status epilepticus Coma Memory impairment Postural instability Muscle cramps Abnormal cerebellum morphology Generalized myoclonic seizures Sensory impairment Increased serum lactate Hip dysplasia Type II diabetes mellitus Specific learning disability Amenorrhea Cerebral calcification Pigmentary retinopathy Generalized-onset seizure Bilateral sensorineural hearing impairment Nephrotic syndrome Areflexia Dystonia Hypopigmentation of the skin Macular edema Hemoptysis Optic neuropathy Joint swelling Increased CSF protein Hypothermia Upper airway obstruction Bone cyst Hyperuricemia Skin nodule Night sweats Anterior synechiae of the anterior chamber Pneumothorax Abnormality of the pleura Vitreous hemorrhage Keratoconjunctivitis sicca Abnormality of the musculature Cystoid macular edema Leukopenia Pancytopenia Abnormal lung morphology Subcutaneous nodule Nephrolithiasis Bronchiectasis Nephrocalcinosis Hypercalcemia Chorioretinal atrophy Portal hypertension Inflammation of the large intestine Epiphora Diabetes insipidus Emphysema Pulmonary fibrosis Blurred vision Chylothorax Abnormality of the cerebrospinal fluid Cerebellar atrophy Pulmonary granulomatosis Abnormal cardiac ventricular function Increased T cell count Abnormality of the nasal mucosa Maculopapular exanthema Enlarged lacrimal glands Vitreous snowballs Abnormal trabecular meshwork morphology Abnormal liver parenchyma morphology Microcephaly Motor delay Hypertension Hyperreflexia Tremor Respiratory insufficiency Myopathy Parotitis Non-caseating epithelioid cell granulomatosis Generalized lymphadenopathy Abnormal salivary gland morphology Skin plaque Abnormality of the lymph nodes Abnormality of the adrenal glands Chorioretinitis Dacryocystitis Anterior uveitis Iridocyclitis Abnormality of T cell physiology Abnormal conjunctiva morphology Vitreous floaters Vitritis Abnormal reproductive system morphology Abnormality of skin morphology Posterior vitreous detachment Enlargement of parotid gland Hypertrophy of the upper limb



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