Congestive heart failure, and Thick eyebrow

Diseases related with Congestive heart failure and Thick eyebrow

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


Top matches:

High match CHAR SYNDROME


Char syndrome is characterized by the triad of patent ductus arteriosus (PDA), facial dysmorphism and hand anomalies.

CHAR SYNDROME Is also known as patent ductus arteriosus with facial dysmorphism and abnormal fifth digits

Related symptoms:

  • Global developmental delay
  • Hearing impairment
  • Hypertelorism
  • Strabismus
  • Abnormal facial shape


SOURCES: ORPHANET OMIM MESH MENDELIAN

More info about CHAR SYNDROME

High match ZIMMERMANN-LABAND SYNDROME


Zimmermann-Laband syndrome (ZLS) is a rare disorder characterized by gingival fibromatosis, coarse facial appearance, and absence or hypoplasia of nails or terminal phalanges of hands and feet.

ZIMMERMANN-LABAND SYNDROME Is also known as laband syndrome|gingival fibromatosis-hepatosplenomegaly-other anomalies syndrome|fibromatosis, gingival, with abnormal fingers, fingernails, nose, and ears, and splenomegaly

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Generalized hypotonia
  • Hearing impairment


SOURCES: ORPHANET OMIM MENDELIAN

More info about ZIMMERMANN-LABAND SYNDROME

High match LARSEN-LIKE SYNDROME, B3GAT3 TYPE


Larsen-like syndrome, B3GAT3 type is a rare, genetic, primary bone dysplasia characterized by laxity, dislocations and contractures of the joints, short stature, foot deformities (e.g. clubfeet), broad tips of fingers and toes, short neck, dysmorphic facial features (hypertelorism, downslanting palpebral fissures, upturned nose with anteverted nares, high arched palate) and various cardiac malformations. Severe disease is associated with multiple fractures, osteopenia, arachnodactyly and blue sclerae. A broad spectrum of additional features, including scoliosis, radio-ulnar synostosis, mild developmental delay, and various eye disorders (glaucoma, amblyopia, hyperopia, astigmatism, ptosis), are also reported.

LARSEN-LIKE SYNDROME, B3GAT3 TYPE Is also known as multiple joint dislocations-short stature-craniofacial dysmorphism-congenital heart defects syndrome|larsen syndrome, autosomal recessive, formerly

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Generalized hypotonia


SOURCES: OMIM MESH ORPHANET MENDELIAN

More info about LARSEN-LIKE SYNDROME, B3GAT3 TYPE

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Other less relevant matches:

High match COFFIN-LOWRY SYNDROME


Coffin-Lowry syndrome (CLS) is a rare genetic neurological disorder characterized by psychomotor and growth retardation, facial dysmorphism, digit abnormalities, and progressive skeletal changes.

COFFIN-LOWRY SYNDROME Is also known as cls

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Generalized hypotonia


SOURCES: MESH OMIM ORPHANET MENDELIAN

More info about COFFIN-LOWRY SYNDROME

High 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

High match HURLER SYNDROME


Hurler syndrome is the most severe form of mucopolysaccharidosis type 1 (MPS1; see this term), a rare lysosomal storage disease, characterized by skeletal abnormalities, cognitive impairment, heart disease, respiratory problems, enlarged liver and spleen, characteristic facies and reduced life expectancy.

HURLER SYNDROME Is also known as mpsih|mps1h|mps1-h|mucopolysaccharidosis type 1h|mucopolysaccharidosis type ih|hurler disease

Related symptoms:

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


SOURCES: OMIM ORPHANET MENDELIAN

More info about HURLER SYNDROME

Low 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

Low match URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME; FCMSU


URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME; FCMSU Is also known as faciocardiomusculoskeletal syndrome, uruguay type|fcms

Related symptoms:

  • Scoliosis
  • Low-set ears
  • Downslanted palpebral fissures
  • Cardiomyopathy
  • Congestive heart failure


SOURCES: OMIM MESH MENDELIAN

More info about URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME; FCMSU

Low match LMNA-RELATED CARDIOCUTANEOUS PROGERIA SYNDROME


LMNA-related cardiocutaneous progeria syndrome is a rare, genetic, premature aging syndrome characterized by adulthood-onset cutaneous manifestations that result in a prematurely aged appearance (i.e. premature thinning and graying of scalp hair, loss of subcutaneous fat, tightening of skin) associated with prominent cardiovascular manifestations, such as accelerated atherosclerosis, calcific valve disease, and cardiomyopathy. Patients present loss of eyebrows and eyelashes in childhood and have a predisposition to develop malignancies.

LMNA-RELATED CARDIOCUTANEOUS PROGERIA SYNDROME Is also known as lcps

Related symptoms:

  • Hypertension
  • Cardiomyopathy
  • Congestive heart failure
  • Sparse hair
  • Ventricular hypertrophy


SOURCES: ORPHANET MENDELIAN

More info about LMNA-RELATED CARDIOCUTANEOUS PROGERIA SYNDROME

Top 5 symptoms//phenotypes associated to Congestive heart failure and Thick eyebrow

Symptoms // Phenotype % cases
Cardiomyopathy Common - Between 50% and 80% cases
Mitral regurgitation Common - Between 50% and 80% cases
Hearing impairment Common - Between 50% and 80% cases
Downslanted palpebral fissures Uncommon - Between 30% and 50% cases
Thick vermilion border Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases


Global developmental delay Scoliosis Abnormal facial shape Muscular hypotonia Seizures Intellectual disability Hypertension Hypertelorism Dilatation Dyspnea Coarse facial features Aortic root aneurysm Short stature Everted lower lip vermilion Sensorineural hearing impairment Cardiomegaly Wide nasal bridge Depressed nasal bridge Arrhythmia Prominent supraorbital ridges Anteverted nares Wide nose Sudden cardiac death Tachycardia Mandibular prognathia Posteriorly rotated ears Hernia Abnormality of the skeletal system Syncope Wide mouth Macrocephaly Ventricular tachycardia Cataract Ventricular hypertrophy Hyperkeratosis Delayed eruption of teeth Synophrys Pectus carinatum Cognitive impairment Left ventricular hypertrophy Emphysema Loss of consciousness Coronary artery atherosclerosis Abnormal mitral valve morphology Palpitations Dilated cardiomyopathy Inguinal hernia Hydrocephalus Frontal bossing Growth delay Abnormal aortic valve morphology Thick lower lip vermilion Kyphoscoliosis Kyphosis Generalized hypotonia Strabismus Low-set ears Protruding ear

Rare Symptoms - Less than 30% cases


Right bundle branch block Absent eyebrow Cutis laxa Palmoplantar keratoderma Hemiplegia Metatarsus adductus Nail dystrophy Restrictive ventilatory defect Erythema Elbow flexion contracture Ventricular arrhythmia Corneal dystrophy Endocardial fibroelastosis Progressive hearing impairment Aortic regurgitation Long eyelashes Aplasia/Hypoplasia of the eyebrow Heart murmur Craniosynostosis Hip dislocation Sparse scalp hair Proptosis Sleep disturbance Osteopenia Pes planus Abnormal heart valve morphology Highly arched eyebrow Genu valgum Abnormal lung morphology Bundle branch block Short metacarpal Right ventricular cardiomyopathy Microdontia Mitral valve prolapse Woolly hair Carious teeth Broad forehead Myopia Peripheral neuropathy Myocardial infarction Headache Thickened calvaria Spinal canal stenosis Abdominal pain Hyperhidrosis Restrictive cardiomyopathy Constipation Depressivity Myelopathy Patent ductus arteriosus Behavioral abnormality Diarrhea Abnormal diaphysis morphology Vomiting Edema Respiratory insufficiency Fatigue Pain Broad palm Hypertrophic cardiomyopathy Glaucoma Long philtrum Skeletal muscle atrophy Optic atrophy Ventricular septal defect Abnormality of the cardiovascular system Intellectual disability, mild Mental deterioration Chest pain Severe global developmental delay Vertigo Stroke Abnormal form of the vertebral bodies Decreased body weight Pruritus Coxa valga Widely spaced teeth Corneal opacity Sleep apnea Polydactyly Cerebral cortical atrophy Lymphedema Pes cavus Coronary artery stenosis Reduced ejection fraction Clubbing of fingers Angina pectoris Protruding tongue Myocardial fibrosis Generalized hirsutism Gingival overgrowth Thickened skin Hypertrichosis Bicuspid aortic valve T-wave inversion Intellectual disability, profound Macroglossia Large earlobe Coarse hair Hirsutism Short distal phalanx of finger Bulbous nose Joint hypermobility Hepatosplenomegaly Umbilical hernia Macrotia Splenomegaly Intellectual disability, severe Brachydactyly Hepatomegaly High palate Hyperextensibility of the finger joints Accelerated skeletal maturation Lumbar kyphosis Hypodontia Flexion contracture Broad nasal tip Micrognathia Midface retrusion Abnormal heart morphology Short neck Exertional dyspnea Delayed skeletal maturation Fever Prominent forehead Abnormal EKG Decreased lacrimation Shortened PR interval Thoracic scoliosis Rhinitis Short clavicles Arthropathy Hypoplasia of the odontoid process Elevated hepatic transaminase Pallor Conductive hearing impairment Flared metaphysis Apnea Palpebral edema Multiple joint contractures Toe walking Joint stiffness Visual loss Stridor Language impairment Back pain Concentric hypertrophic cardiomyopathy Recurrent upper respiratory tract infections Angiokeratoma corporis diffusum Abnormality of the elbow Protuberant abdomen Papillary renal cell carcinoma Abnormality of the respiratory system Dysostosis multiplex Diastasis recti Gingivitis Nephrogenic diabetes insipidus Decreased glomerular filtration rate Vascular tortuosity Distal renal tubular acidosis Abnormality of the clavicle Increased blood urea nitrogen Reduced sperm motility Angiokeratoma Pneumonia Obstructive lung disease Impaired temperature sensation Hyposthenuria Loss of eyelashes Abnormality of the skull Obstructive sleep apnea Recurrent lower respiratory tract infections Shortened QT interval Skeletal dysplasia Retinopathy Shallow orbits Peripheral visual field loss Increased intracranial pressure Abnormal glomerular filtration rate Hyperammonemia Delayed speech and language development Left ventricular septal hypertrophy Hip dysplasia Abnormality of the skin Tenesmus Limitation of joint mobility Asthma Full cheeks Neurodegeneration Nyctalopia High, narrow palate Dolichocephaly Heavy proteinuria Acroparesthesia Progressive visual loss Feeding difficulties Inability to walk Abnormality of skin pigmentation Abnormal common carotid artery morphology Cornea verticillata Abnormal ST segment Increased carotid artery intimal medial thickness Increased glomerular filtration rate Retinal degeneration Tracheal stenosis Abnormality of the common coagulation pathway Dry skin Tortuosity of conjunctival vessels Aortic atherosclerosis Cerebral palsy ST segment depression Abnormality of eye movement Camptodactyly of finger Opacification of the corneal stroma Pulmonary carcinoid tumor Mucosal telangiectasiae Abnormality of the dentition Abnormality of dental enamel Spastic paraparesis Abnormal pyramidal sign Abnormal vertebral morphology Exotropia Unexplained fevers Recurrent respiratory infections Hyperkeratotic papule Functional abnormality of the gastrointestinal tract Impaired renal concentrating ability Abnormality of glycosphingolipid metabolism Abnormality of epiphysis morphology Abnormality of the forehead Chronic diarrhea Encephalocele Split hand Recurrent otitis media Progressive neurologic deterioration Interphalangeal joint contracture of finger Lumbar hyperlordosis Abnormality of the ribs Coxa vara Flared nostrils Beaking of vertebral bodies Cardiac arrest Cleft upper lip Sepsis Ectodermal dysplasia Abnormal blistering of the skin Cyanosis Epidermal acanthosis Sparse and thin eyebrow Acanthosis nigricans Alopecia Brittle hair Prematurely aged appearance Akinesia Scleroderma Lipoatrophy Fragile skin Curly hair Respiratory failure Agenesis of molar Ventricular extrasystoles Hypokinesia Abnormal mandible coronoid process morphology Abnormality of premolar morphology Abnormal mandibular ramus morphology Delayed ossification of the hand bones Ichthyosis Oligodontia Reduced number of teeth Agenesis of permanent teeth Gingival recession Parakeratosis Premature skin wrinkling Fragile nails Absent eyelashes Leukonychia Selective tooth agenesis Reduced systolic function Alopecia of scalp Onycholysis Abnormality of the tympanic membrane Hypercholesterolemia Limited elbow movement Brachyturricephaly Basal cell carcinoma Hyperplasia of the maxilla Premature graying of hair Intracranial hemorrhage Camptodactyly of toe Atherosclerosis Hallux valgus Aortic valve stenosis Hypertriglyceridemia Sparse hair Dislocation of toes Pugilistic facies Marked muscular hypertrophy Broad nail Eclabion Skeletal muscle hypertrophy Hypergranulosis Ventricular flutter Abnormality of hair texture Acantholysis Abnormal T-wave Prolonged QRS complex Right ventricular dilatation Paroxysmal ventricular tachycardia Abnormal right ventricle morphology Reduced subcutaneous adipose tissue Abnormality of the voice Abnormal morphology of right ventricular trabeculae Elevated serum creatine phosphokinase Retrognathia Difficulty walking Prominent nose Joint contracture of the hand Congenital hip dislocation Stiff interphalangeal joints Abnormality of glycosaminoglycan metabolism Communicating hydrocephalus Abnormal nerve conduction velocity Chronic rhinitis Biconcave vertebral bodies Mucopolysacchariduria Large face Squamous cell carcinoma of the skin Sclerosis of skull base Difficulty standing Anterior open bite Recurrent ear infections Meckel diverticulum Narrow pelvis bone Progressive pes cavus Large sella turcica Anterior rib cupping Prominent sternum J-shaped sella turcica Retinal fold Diaphyseal thickening Atlantoaxial dislocation Seborrheic dermatitis Upper airway obstruction Hypoplastic ilia Conical tooth Cor pulmonale Flared iliac wings Foam cells Pulmonary edema Constrictive median neuropathy Delayed ossification of carpal bones Hypoplasia of teeth Sagittal craniosynostosis Mitral valve calcification Abnormality of peripheral nerve conduction Rhinorrhea Abnormality of the pulmonary artery Broad femoral neck Abnormality of the gingiva Hip subluxation Increased size of nasopharyngeal adenoids Abnormality of joint mobility Enlarged tonsils Hypoplastic cervical vertebrae Cervical subluxation Mandibular condyle hypoplasia Abnormality of lysosomal metabolism Flaring of rib cage Broad ischia Delayed tarsal ossification Abnormality of the tonsils Thick skull base Deformed humerus Enlarged vertebral pedicles Proximal tapering of metacarpals Bullet-shaped phalanges of the hand Broad long bone diaphyses Abnormality of the wing of the ilium C1-C2 subluxation Calcification of falx cerebri Heparan sulfate excretion in urine Hernia of the abdominal wall Abnormal hand morphology Enlargement of the wrists Abnormality of the middle ear ossicles Cervical myelopathy Calvarial hyperostosis Thoracolumbar kyphoscoliosis Alopecia universalis Urinary glycosaminoglycan excretion Hypoplasia of the femoral head Short mandibular rami Cervical kyphosis Abnormal CNS myelination Dermatan sulfate excretion in urine Limb pain Abnormality of mucopolysaccharide metabolism Abnormality of the pubic bone Abnormality of temperature regulation Hyperlipidemia Corneal crystals Generalized osteoporosis Congenital glaucoma Narrow nasal bridge Upper limb undergrowth Abnormally large globe Overlapping fingers 11 pairs of ribs Small face Bilateral talipes equinovarus Deep palmar crease Abnormality of the abdominal wall Lumbar scoliosis Knee dislocation Talipes equinovalgus Multiple joint dislocation Thoracic hypoplasia Spondyloepiphyseal dysplasia Hypertropia Amblyopia Recurrent fractures Esotropia Webbed neck Congenital diaphragmatic hernia Low posterior hairline Blue sclerae Rhizomelia Radioulnar synostosis Meningitis Joint dislocation Microretrognathia Sandal gap Hyperextensible skin Patent foramen ovale Shoulder dislocation Accessory carpal bones Arachnodactyly Cerebellar vermis hypoplasia Tapered finger Single transverse palmar crease Hypoplasia of the maxilla Tetraplegia Dental malocclusion Psychosis Open mouth Neurological speech impairment Abnormality of retinal pigmentation Wide anterior fontanel Abnormality of the hair Narrow palate Aplasia/Hypoplasia of the corpus callosum Schizophrenia Joint hyperflexibility Hyperlordosis Enlarged metaphyses Muscle weakness Prominent antitragus Spatulate thumbs Broad distal phalanges of all fingers Metacarpophalangeal joint hyperextensibility Bilateral elbow dislocations Microcephaly Epicanthus Feeding difficulties in infancy Gait disturbance Ventriculomegaly Hypoplasia of the corpus callosum Hypertonia Pectus excavatum Telecanthus Flat face Talipes Self-injurious behavior Symphalangism of the 5th finger Persistence of primary teeth Triangular mouth Mesoaxial hand polydactyly No permanent dentition Parasomnia Muscular ventricular septal defect Mesoaxial foot polydactyly Prominent occiput Distal/middle symphalangism of 5th finger Polyhydramnios Congenital cataract Overgrowth Bilateral sensorineural hearing impairment Small nail Short middle phalanx of the 5th finger Supernumerary nipple Hemivertebrae Clinodactyly of the 5th finger Ptosis Short nose Malar flattening Syndactyly Abnormality of cardiovascular system morphology Clinodactyly High forehead Hand polydactyly Short philtrum Toe syndactyly Premature birth Coarctation of aorta Depressed nasal ridge Finger clinodactyly Nephrolithiasis Intellectual disability, progressive Abnormality of the foot Brachycephaly Mesiodens Cleft palate Motor delay Talipes equinovarus Respiratory distress Osteoporosis Narrow mouth Prominent eyelashes Joint laxity Abnormal cardiac septum morphology Microtia Hypermetropia Narrow chest Pulmonic stenosis Short distal phalanx of toe Aortic arch aneurysm Spina bifida occulta Broad ribs Hemangioma Growth abnormality Metaphyseal widening Large for gestational age Anonychia Pericardial effusion Dystrophic fingernails Everted upper lip vermilion Thin bony cortex Colpocephaly Long penis Gingival fibromatosis Cavernous hemangioma Biliary atresia Generalized hypertrichosis Redundant skin Abnormality of dental morphology Retinal vascular tortuosity Glycosuria Interstitial pulmonary abnormality Progressive sensorineural hearing impairment Orthostatic hypotension Celiac disease Telangiectasia of the skin Glomerulopathy Renal tubular acidosis Impotence Wheezing Abnormality of lipid metabolism Xerostomia Transient ischemic attack Renal tubular dysfunction Edema of the lower limbs Elevated erythrocyte sedimentation rate Anhidrosis Elevated serum creatinine Abnormality of the hand Ischemic stroke Reduced bone mineral density Tinnitus Easy fatigability Atrioventricular block Chronic kidney disease Glomerulosclerosis Polyuria Polydipsia Personality changes Clubbing Impaired vibratory sensation Tricuspid regurgitation Diabetes insipidus Tubulointerstitial nephritis Tubular atrophy Purpura Conjunctival telangiectasia Tubulointerstitial fibrosis Abnormal thrombosis Abnormality of the renal tubule Abnormal cornea morphology Dysesthesia Supraventricular arrhythmia Microalbuminuria Abnormal renal physiology Primary hypothyroidism Biventricular hypertrophy Abnormal endocardium morphology Abnormality of cardiovascular system physiology Decreased female libido Vascular skin abnormality Chronic pain Miosis Abnormality of the gastrointestinal tract Sinus bradycardia Oligospermia Supraventricular tachycardia Heat intolerance Peripheral arterial stenosis Chronic obstructive pulmonary disease Achalasia Chronic fatigue Gastrointestinal dysmotility Abnormality of femur morphology Abnormality of the nose Abnormal myocardium morphology High-frequency hearing impairment Asymmetric septal hypertrophy Periorbital fullness Abnormal intestine morphology Aminoaciduria Aplasia/Hypoplasia of the cerebellum Pseudoepiphyses of the metacarpals Narrow iliac wings Broad finger Abnormal tricuspid valve morphology Hyperconvex fingernails Cataplexy Stooped posture Retinoschisis Premature loss of primary teeth Uterine prolapse Bifid sternum Thick nasal septum Abnormality of the nasal alae Drumstick terminal phalanges Anemia Thick nasal alae Rectal prolapse Hypothyroidism Atonic seizures Large hands Cutis marmorata Abnormality of neuronal migration Broad hallux Progressive spasticity Abnormality of digit Anteriorly placed anus Advanced eruption of teeth Severe sensorineural hearing impairment Soft skin Acrocyanosis Hypoplastic fingernail Craniofacial hyperostosis Delayed closure of the anterior fontanelle Renal insufficiency Arthralgia Exercise intolerance Atrial fibrillation Nephropathy Muscle cramps Abdominal distention Urinary incontinence Hypotension Nephrotic syndrome Subcutaneous nodule Nausea Anorexia Hypohidrosis Bradycardia Fasciculations Abnormal autonomic nervous system physiology Spontaneous abortion Hematuria Stage 5 chronic kidney disease Myalgia Developmental regression Carcinoma Arthritis Anxiety Proteinuria Abnormality of the nervous system Abnormality of the kidney Skin rash Paresthesia Cough Prominent nasal bridge Papule Abnormality of the cerebral white matter Malabsorption Nausea and vomiting Delayed puberty Abnormality of the intrahepatic bile duct



If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like Hepatomegaly and Frontal bossing, related diseases and genetic alterations Congestive heart failure and Progressive cerebellar ataxia, related diseases and genetic alterations Fever and Atrial septal defect, related diseases and genetic alterations Lymphoma and Prostate cancer, related diseases and genetic alterations Ptosis and Distal muscle weakness, related diseases and genetic alterations Strabismus and Postaxial hand polydactyly, related diseases and genetic alterations

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