Congestive heart failure, and Subcutaneous nodule

Diseases related with Congestive heart failure and Subcutaneous nodule

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


Top matches:

Medium match SEGMENTAL OUTGROWTH-LIPOMATOSIS-ARTERIOVENOUS MALFORMATION-EPIDERMAL NEVUS SYNDROME


Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome is a rare, genetic, polymalformative syndrome characterized by progressive, proportionate, asymmetric segmental overgrowth (with soft tissue hypertrophy and ballooning effect) that develops and progresses rapidly in early childhood, arteriovenous and lymphatic vascular malformations, lipomatosis and linear epidermal nevus (arranged in whorls along the lines of Blaschko). Clinical symptoms of Cowden syndrome, such as macrocephaly and progressive development of numerous hypertrophic hamartomatous and neoplastic lesions involving multiple organs and systems, are also associated. Patients present an increased risk of developing cancer.

SEGMENTAL OUTGROWTH-LIPOMATOSIS-ARTERIOVENOUS MALFORMATION-EPIDERMAL NEVUS SYNDROME Is also known as solamen syndrome

Related symptoms:

  • Macrocephaly
  • Congestive heart failure
  • Papule
  • Talipes
  • Recurrent fractures


SOURCES: ORPHANET MENDELIAN

More info about SEGMENTAL OUTGROWTH-LIPOMATOSIS-ARTERIOVENOUS MALFORMATION-EPIDERMAL NEVUS SYNDROME

Medium match NAKAJO-NISHIMURA SYNDROME


Nakajo-Nishimura syndrome (NNS) is a rare autoinflammatory disorder belonging to the proteasome disability syndrome (see this term) group, and characterized by pernio-like lesions appearing in infancy followed by recurrent fever, nodular skin eruption, partial lipodystrophy (mainly in upper extremities and face) and joint contractures.

NAKAJO-NISHIMURA SYNDROME Is also known as nns|secondary hypertrophic osteoperiostosis with pernio|amyotrophy-fat tissue anomaly syndrome

Related symptoms:

  • Muscle weakness
  • Hepatomegaly
  • Fever
  • Skeletal muscle atrophy
  • Respiratory insufficiency


SOURCES: ORPHANET MENDELIAN

More info about NAKAJO-NISHIMURA SYNDROME

Medium match CARNEY COMPLEX


Carney complex (CNC) is characterized by spotty skin pigmentation, endocrine overactivity and myxomas.

CARNEY COMPLEX Is also known as myxoma-spotty pigmentation-endocrine overactivity syndrome|carney syndrome|carney myxoma-endocrine complex, type 2

Related symptoms:

  • Neoplasm
  • Congestive heart failure
  • Stroke
  • Hirsutism
  • Sudden cardiac death


SOURCES: ORPHANET OMIM MENDELIAN

More info about CARNEY COMPLEX

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Other less relevant matches:

Medium match PSEUDOXANTHOMA ELASTICUM


Pseudoxanthoma elasticum (PXE) is an inherited connective tissue disorder characterized by progressive calcification and fragmentation of elastic fibers in the skin, retina, and arterial walls.

PSEUDOXANTHOMA ELASTICUM Is also known as pxe|gronblad-strandberg-touraine syndrome|gronblad-strandberg syndrome

Related symptoms:

  • Scoliosis
  • Growth delay
  • High palate
  • Visual impairment
  • Hypertension


SOURCES: ORPHANET OMIM MENDELIAN

More info about PSEUDOXANTHOMA ELASTICUM

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 FIBRODYSPLASIA OSSIFICANS PROGRESSIVA


Fibrodysplasia ossificans progressiva (FOP) is a severely disabling heritable disorder of connective tissue characterized by congenital malformations of the great toes and progressive heterotopic ossification that forms qualitatively normal bone in characteristic extraskeletal sites.

FIBRODYSPLASIA OSSIFICANS PROGRESSIVA Is also known as stone man syndrome|fop|myositis ossificans progressiva

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Hearing impairment
  • Scoliosis


SOURCES: OMIM ORPHANET MENDELIAN

More info about FIBRODYSPLASIA OSSIFICANS PROGRESSIVA

Medium match TUBEROUS SCLEROSIS 1; TSC1


Tuberous sclerosis complex (TSC) is an autosomal dominant multisystem disorder characterized by hamartomas in multiple organ systems, including the brain, skin, heart, kidneys, and lung. Central nervous system manifestations include epilepsy, learning difficulties, behavioral problems, and autism. Renal lesions, usually angiomyolipomas, can cause clinical problems secondary to hemorrhage or by compression and replacement of healthy renal tissue, which can cause renal failure. Patients can also develop renal cysts and renal-cell carcinomas. Pulmonary lymphangioleiomyomatosis can develop in the lungs. Skin lesions include melanotic macules, facial angiofibromas, and patches of connective tissue nevi. There is a wide clinical spectrum, and some patients may have minimal symptoms with no neurologic disability (reviews by Crino et al., 2006 and Curatolo et al., 2008). Genetic Heterogeneity of Tuberous SclerosisSee also tuberous sclerosis-2 (OMIM ), which is caused by mutation in the TSC2 gene (OMIM ) on chromosome 16p13.Approximately 10 to 30% of cases of tuberous sclerosis are due to mutations in the TSC1 gene: the frequency of cases due to mutations in the TSC2 gene is consistently higher. TSC2 mutations are associated with more severe disease (Crino et al., 2006) (see GENOTYPE/PHENOTYPE CORRELATIONS section).

TUBEROUS SCLEROSIS 1; TSC1 Is also known as tuberous sclerosis complex|ts|tuberose sclerosis|tsc

Related symptoms:

  • Intellectual disability
  • Seizures
  • Neoplasm
  • Pain
  • Hypertension


SOURCES: OMIM MENDELIAN

More info about TUBEROUS SCLEROSIS 1; TSC1

Medium 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

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

Low match WELL-DIFFERENTIATED LIPOSARCOMA


Well-differentiated liposarcoma (WDLS), the most common type of liposarcoma (LS; see this term), is a slow growing, painless tumor usually located in the retroperitoneum or the limbs. It is composed of proliferating mature adipocytes.

WELL-DIFFERENTIATED LIPOSARCOMA Is also known as alt|atypical lipoma|wdls|atypical lipomatous tumor

Related symptoms:

  • Subcutaneous nodule
  • Gastrointestinal dysmotility
  • Abnormal renal physiology


SOURCES: ORPHANET MENDELIAN

More info about WELL-DIFFERENTIATED LIPOSARCOMA

Top 5 symptoms//phenotypes associated to Congestive heart failure and Subcutaneous nodule

Symptoms // Phenotype % cases
Arrhythmia Uncommon - Between 30% and 50% cases
Renal insufficiency Uncommon - Between 30% and 50% cases
Papule Uncommon - Between 30% and 50% cases
Seizures Uncommon - Between 30% and 50% cases
Hypothyroidism Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases


Fever Skin rash Dilatation Sudden cardiac death Hamartoma Pain Stroke Neoplasm Respiratory insufficiency Elevated erythrocyte sedimentation rate Chest pain Edema Hypertension Cafe-au-lait spot Emphysema Cough Glaucoma Behavioral abnormality Intellectual disability Headache Cerebral calcification Dyspnea Anemia Pneumothorax Myocardial infarction Intellectual disability, mild Chylothorax

Rare Symptoms - Less than 30% cases


Abnormal renal physiology Abnormality of the gastrointestinal tract Astrocytoma Gingival fibromatosis Gastrointestinal dysmotility Abnormality of the pleura Ependymoma Visual impairment Chordoma Arthritis Scoliosis Angiofibromas Renal angiomyolipoma Adenoma sebaceum Optic nerve glioma Shagreen patch Abnormal endocardium morphology Abnormal mitral valve morphology Atrioventricular block Cortical tubers Abnormality of the cardiovascular system Tricuspid regurgitation Chorioretinal atrophy Sensorineural hearing impairment Rhabdomyoma Ischemic stroke Telangiectasia of the skin Subungual fibromas Achromatic retinal patches Nephrocalcinosis Mitral regurgitation Pulmonary lymphangiomyomatosis Mitral valve prolapse Alopecia Restrictive cardiomyopathy Ungual fibroma Respiratory failure Dental enamel pits Pruritus Hypomelanotic macule Cardiac rhabdomyoma Scarring Peripheral arterial stenosis Angina pectoris Subependymal nodules Hyperkeratotic papule Blindness Cardiomyopathy Tubulointerstitial nephritis Respiratory distress Osteochondroma Hepatomegaly Ventricular tachycardia Thick lower lip vermilion Cardiomegaly Autism Lymphadenopathy Anxiety Anorexia Attention deficit hyperactivity disorder Arthralgia Precocious puberty Hyperhidrosis Splenomegaly Skeletal muscle atrophy Abnormal lung morphology Increased antibody level in blood Palpitations Renal cyst Syncope Neoplasm of the breast Excessive wrinkled skin Specific learning disability Cataract Peripheral neuropathy Fatigue Ovarian neoplasm Hemiplegia/hemiparesis Reduced bone mineral density Generalized-onset seizure Bradycardia Optic atrophy Hearing impairment Cognitive impairment Skin tags Carcinoma Infantile spasms Coronary artery atherosclerosis Abnormality of the kidney Interstitial pulmonary abnormality Neoplasm of the pancreas Abnormality of the cerebral white matter Renal cell carcinoma Nausea Hypermelanotic macule Abnormality of the respiratory system Wolff-Parkinson-White syndrome Diabetes insipidus Nevus Hypopigmentation of the skin Erythema nodosum Clubbing of fingers Global developmental delay Vomiting Constipation Posteriorly rotated ears Abdominal pain Midface retrusion Mandibular prognathia Hyperkeratosis Diarrhea Depressivity Pulmonary granulomatosis Short stature Abnormal trabecular meshwork morphology Proteinuria Coarse facial features Myalgia Macrocephaly Vitreous snowballs Inflammation of the large intestine Hypothermia Increased CSF protein Heart block Joint swelling Uveitis Optic neuropathy Hemoptysis Keratoconjunctivitis sicca Hyperuricemia Hyperthyroidism Abnormality of the musculature Blurred vision Pulmonary fibrosis Epiphora Pleural effusion Macular edema Portal hypertension Hypercalcemia Hypercalciuria Eosinophilia Leukopenia Osteolysis Decreased liver function Hyperpigmentation of the skin Bronchiectasis Nephrolithiasis Pancytopenia Hemolytic anemia Hepatic failure Erythema Upper airway obstruction Immune dysregulation Enlarged lacrimal glands Abnormal conjunctiva morphology Maculopapular exanthema Abnormality of the nasal mucosa Increased T cell count Abnormal cardiac ventricular function Parotitis Abnormal liver parenchyma morphology Non-caseating epithelioid cell granulomatosis Abnormality of T cell physiology Enlargement of parotid gland Posterior vitreous detachment Abnormality of skin morphology Abnormal reproductive system morphology Vitritis Vitreous floaters Abnormality of the nervous system Bone cyst Abnormal salivary gland morphology Anterior uveitis Dacryocystitis Chorioretinitis Abnormality of the adrenal glands Abnormality of the lymph nodes Skin plaque Generalized lymphadenopathy Abnormality of the cerebrospinal fluid Cystoid macular edema Vitreous hemorrhage Anterior synechiae of the anterior chamber Night sweats Skin nodule Iridocyclitis Hypohidrosis Hypertrophic cardiomyopathy Microalbuminuria Abnormal thrombosis Abnormality of the renal tubule Abnormal cornea morphology Dysesthesia Supraventricular arrhythmia Conjunctival telangiectasia Primary hypothyroidism Chronic pain Biventricular hypertrophy Abnormality of cardiovascular system physiology Decreased female libido Vascular skin abnormality Retinal vascular tortuosity Corneal crystals Tubulointerstitial fibrosis Miosis Abnormality of temperature regulation Chronic fatigue Heat intolerance Reduced ejection fraction Chronic obstructive pulmonary disease Achalasia Sinus bradycardia Myocardial fibrosis Abnormality of femur morphology T-wave inversion Abnormality of the nose Abnormal myocardium morphology High-frequency hearing impairment Asymmetric septal hypertrophy Periorbital fullness Abnormal aortic valve morphology Limb pain Nephrogenic diabetes insipidus Large earlobe Heavy proteinuria Impaired renal concentrating ability Abnormality of glycosphingolipid metabolism Abnormality of the forehead Tortuosity of conjunctival vessels Left ventricular septal hypertrophy Tenesmus Acroparesthesia ST segment depression Abnormal common carotid artery morphology Abnormal ST segment Increased carotid artery intimal medial thickness Increased glomerular filtration rate Abnormality of the common coagulation pathway Abnormal glomerular filtration rate Functional abnormality of the gastrointestinal tract Unexplained fevers Decreased glomerular filtration rate Impaired temperature sensation Vascular tortuosity Distal renal tubular acidosis Increased blood urea nitrogen Reduced sperm motility Angiokeratoma Obstructive lung disease Hyposthenuria Mucosal telangiectasiae Shortened QT interval Angiokeratoma corporis diffusum Decreased lacrimation Shortened PR interval Coronary artery stenosis Concentric hypertrophic cardiomyopathy Supraventricular tachycardia Oligospermia Developmental regression Abnormal autonomic nervous system physiology Nephrotic syndrome Ventricular hypertrophy Atrial fibrillation Left ventricular hypertrophy Lymphedema Fasciculations Spontaneous abortion Urinary incontinence Exercise intolerance Aminoaciduria Purpura Hyperlipidemia Aortic regurgitation Abnormal intestine morphology Hypotension Abdominal distention Corneal dystrophy Vertigo Prominent nasal bridge Corneal opacity Malabsorption Nausea and vomiting Delayed puberty Paresthesia Stage 5 chronic kidney disease Muscle cramps Tachycardia Bulbous nose Thick eyebrow Thick vermilion border Hematuria Nephropathy Progressive hearing impairment Ventricular arrhythmia Tubular atrophy Aortic root aneurysm Celiac disease Glomerulopathy Abnormal heart valve morphology Glycosuria Renal tubular acidosis Wheezing Abnormality of lipid metabolism Progressive sensorineural hearing impairment Abnormal EKG Xerostomia Transient ischemic attack Renal tubular dysfunction Edema of the lower limbs Elevated serum creatinine Orthostatic hypotension Impotence Tinnitus Polydipsia Easy fatigability Chronic kidney disease Prominent supraorbital ridges Abnormality of the hand Hemiplegia Glomerulosclerosis Personality changes Bundle branch block Heart murmur Clubbing Impaired vibratory sensation Polyuria Anhidrosis Loss of consciousness Facial palsy Broad neck Proximal muscle weakness Growth delay Bruising susceptibility Abnormality of skin pigmentation Joint hyperflexibility Small for gestational age Retinopathy Reduced visual acuity Visual loss Abnormality of cardiovascular system morphology Intrauterine growth retardation Myopia High palate Intra-oral hyperpigmentation Gastrointestinal hemorrhage Abnormality of circulating adrenocorticotropin level Thyroid follicular hyperplasia Sertoli cell neoplasm Pigmentation of the sclera Abnormal pigmentation of the oral mucosa Peripheral Schwannoma Profuse pigmented skin lesions Blue nevus Hepatocellular adenoma Pigmented micronodular adrenocortical disease Cardiac myxoma Histiocytoma Postural instability Abnormality of the skin Uterine neoplasm Severe intrauterine growth retardation Pulmonary insufficiency Arteriosclerosis Arterial stenosis Pulmonary edema Abnormal thrombocyte morphology Redundant neck skin Lack of skin elasticity Abnormality of the cerebral vasculature Mitral stenosis Drusen Thickened nuchal skin fold Abnormality of the mouth Severe vision loss Blue sclerae Striae distensae Multiple lipomas Abnormal retinal morphology Cutis marmorata Acne Abnormality of the thorax Intracranial hemorrhage Redundant skin Hyperextensible skin Cutis laxa Atherosclerosis Macular degeneration Bronchogenic cyst Hypertension associated with pheochromocytoma Choroidal neovascularization Arthrogryposis multiplex congenita Abnormality of the Leydig cells Clubbing of toes Episodic fever Lipoatrophy Microcytic anemia Right bundle branch block Hyperostosis Lipodystrophy Abnormality of the face Prominent nose Macroglossia Arachnodactyly Abnormal pyramidal sign Neoplasm of the skin Joint stiffness Macrotia Muscle weakness Neoplasm of the thyroid gland Upper limb asymmetry Lymphangioma Visceral angiomatosis Venous insufficiency Lower limb asymmetry Arteriovenous malformation Recurrent fractures Talipes Hirsutism Polycystic ovaries Nodular goiter Enlarged polycystic ovaries Vestibular Schwannoma Fibroadenoma of the breast Increased urinary cortisol level Adrenal pheochromocytoma Pituitary growth hormone cell adenoma Abnormal prolactin level Recurrent paroxysmal headache Pancreatic adenocarcinoma Thyroid adenoma Adrenocortical carcinoma Testicular neoplasm Pituitary prolactin cell adenoma Multiple lentigines Colon cancer Schwannoma Red hair Hypoplasia of the musculature Stomach cancer Ovarian cyst Parathyroid adenoma Thyroid carcinoma Neoplasm of the endocrine system Pituitary adenoma Prolactin excess Increased circulating cortisol level Growth hormone excess Ectopic calcification Retinal hemorrhage Photophobia Stiff neck Abnormality of the first metatarsal bone Progressive cervical vertebral spine fusion Ectopic ossification in tendon tissue Ectopic ossification in ligament tissue Ectopic ossification in muscle tissue Small cervical vertebral bodies Ectopic ossification Fibrosarcoma Synostosis of joints Soft tissue sarcoma Low-grade fever Overbite Broad femoral neck Hydrocephalus Short 1st metacarpal Short hallux Myositis Exostoses Ankylosis Alopecia of scalp Basal ganglia calcification Spinal rigidity Hallux valgus Metaphyseal widening Back pain Sarcoma Aplasia/Hypoplasia of the phalanges of the hallux Hyperactivity Finger clinodactyly Nephroblastoma Weight loss Thrombocytopenia Projection of scalp hair onto lateral cheek Connective tissue nevi Premature chromatid separation Flank pain Fibroma Brain neoplasm White hair Renal neoplasm Generalized hypopigmentation Hyperventilation Aortic aneurysm Intellectual disability, moderate Polycystic kidney dysplasia CNS hypomyelination Tachypnea Hypoplasia of dental enamel Heterotopia Focal-onset seizure Brain atrophy Gliosis Sleep disturbance Retinal detachment Autistic behavior Irritability Widely spaced teeth Aspiration Intermittent claudication Peau d'orange Hypopigmented skin patches Aplasia/Hypoplasia of the corpus callosum Iris coloboma Abnormality of the liver EEG abnormality Motor delay Medial calcification of small arteries Abnormal atrioventricular valve morphology Medial calcification of medium-sized arteries Premature occlusive vascular stenosis Erythematous papule Subretinal fluid Peripapillary chorioretinal atrophy Abnormality of neuronal migration Medial calcification of large arteries Generalized arterial calcification Localized skin lesion Arterial calcification Subcutaneous calcification Vascular calcification Accelerated atherosclerosis Civatte bodies Abnormality of connective tissue Renovascular hypertension Metamorphopsia Angioid streaks of the fundus Increased intracranial pressure Prominent occiput Abnormal vertebral morphology Low-set ears Short thumb Limitation of joint mobility Hypotrichosis Respiratory tract infection Conductive hearing impairment Difficulty walking Pneumonia Clinodactyly of the 5th finger Clinodactyly Kyphosis Abnormality of the skeletal system Flexion contracture Failure to thrive Cortical dysplasia Subependymal giant-cell astrocytoma Confetti-like hypopigmented macules Retinal hamartoma Macrodactyly Third degree atrioventricular block Rhabdomyosarcoma Abnormality of the pancreas Gingivitis Multiple renal cysts Nevus flammeus Multiple cafe-au-lait spots Macule Cornea verticillata



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