Congestive heart failure, and Clinodactyly of the 5th finger

Diseases related with Congestive heart failure and Clinodactyly of the 5th finger

In the following list you will find some of the most common rare diseases related to Congestive heart failure and Clinodactyly of the 5th finger that can help you solving undiagnosed cases.


Top matches:

Medium match TETRALOGY OF FALLOT


Tetralogy of Fallot is a congenital cardiac malformation that consists of an interventricular communication, also known as a ventricular septal defect, obstruction of the right ventricular outflow tract, override of the ventricular septum by the aortic root, and right ventricular hypertrophy.

Related symptoms:

  • Growth delay
  • Muscle weakness
  • Cryptorchidism
  • Anemia
  • Brachydactyly


SOURCES: OMIM MESH ORPHANET MENDELIAN

More info about TETRALOGY OF FALLOT

Medium 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

Medium match AARSKOG-SCOTT SYNDROME


Aarskog-Scott syndrome (AAS) is a rare developmental disorder characterized by facial, limbs and genital features, and a disproportionate acromelic short stature.

AARSKOG-SCOTT SYNDROME Is also known as aarskog syndrome|faciodigitogenital syndrome|faciogenital dysplasia

Related symptoms:

  • Short stature
  • Hypertelorism
  • Strabismus
  • Cleft palate
  • Cryptorchidism


SOURCES: ORPHANET MENDELIAN

More info about AARSKOG-SCOTT SYNDROME

Mendelian

Too many results?
We can help you with your rare disease diagnosis.

Learn more

Other less relevant matches:

Medium match ARTERIAL TORTUOSITY SYNDROME


Arterial tortuosity syndrome (ATS) is a rare connective tissue disorder characterized by tortuosity and elongation of the large and medium-sized arteries and a propensity towards aneurysm formation, vascular dissection, and stenosis of the pulmonary arteries.

ARTERIAL TORTUOSITY SYNDROME Is also known as ats

Related symptoms:

  • Intellectual disability
  • Global developmental delay
  • Scoliosis
  • Hypertelorism
  • Strabismus


SOURCES: ORPHANET MENDELIAN

More info about ARTERIAL TORTUOSITY SYNDROME

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 TEMTAMY SYNDROME


Temtamy syndrome is a very rare congenital genetic neurological disorder characterized by agenesis/hypoplasia of corpus callosum with developmental abnormalities, ocular disorders, and variable craniofacial and skeletal abnormalities.

TEMTAMY SYNDROME Is also known as temtamy-shalash syndrome|craniofacial dysmorphism-coloboma-corpus callosum agenesis syndrome|mental retardation with or without craniofacial dysmorphism, ocular coloboma, or abnormal corpus callosum

Related symptoms:

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


SOURCES: ORPHANET MESH OMIM MENDELIAN

More info about TEMTAMY SYNDROME

Medium match ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS


Andersen-Tawil syndrome is an autosomal dominant multisystem channelopathy characterized by periodic paralysis, ventricular arrhythmias, and distinctive dysmorphic facial or skeletal features. Hypoplastic kidney and valvular heart disease have also been reported. The disorder shows marked intrafamilial variability and incomplete penetrance (summary by Davies et al., 2005).

ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS Is also known as ats|andersen syndrome|long qt syndrome 7|periodic paralysis, potassium-sensitive cardiodysrhythmic type|lqt7|andersen-tawil syndrome

Related symptoms:

  • Seizures
  • Short stature
  • Microcephaly
  • Scoliosis
  • Ataxia


SOURCES: OMIM MENDELIAN

More info about ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS

Medium match FRANK-TER HAAR SYNDROME


Frank-ter Haar syndrome (formerly considered as an autosomal recessive form of Melnick-Needles syndrome; see this term) is defined by megalocornea, multiple skeletal anomalies, characteristic facial dysmorphism (wide fontanels, prominent forehead, hypertelorism, prominent eyes, full cheeks and micrognathia) and developmental delay.

FRANK-TER HAAR SYNDROME Is also known as ter haar syndrome|borrone dermatocardioskeletal syndrome|melnick-needles syndrome, autosomal recessive, formerly

Related symptoms:

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


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about FRANK-TER HAAR SYNDROME

Medium match CRANIOECTODERMAL DYSPLASIA


Cranioectodermal dysplasia (CED) is a rare developmental disorder characterized by congenital skeletal and ectodermal defects associated with dysmorphic features, nephronophthisis, hepatic fibrosis and ocular anomalies (mainly retinitis pigmentosa).

CRANIOECTODERMAL DYSPLASIA Is also known as levin syndrome i|sensenbrenner syndrome|ced

Related symptoms:

  • Global developmental delay
  • Generalized hypotonia
  • Microcephaly
  • Growth delay
  • Nystagmus


SOURCES: OMIM ORPHANET MENDELIAN

More info about CRANIOECTODERMAL DYSPLASIA

Medium match ROBERTS SYNDROME


Roberts syndrome (RBS) is characterized by pre- and postnatal growth retardation, severe symmetric limb reduction defects, craniofacial anomalies and severe intellectual deficit. SC phocomelia is a milder form of RBS.

ROBERTS SYNDROME Is also known as pseudothalidomide syndrome|roberts-sc phocomelia syndrome|sc pseudothalidomide syndrome|sc phocomelia

Related symptoms:

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


SOURCES: OMIM ORPHANET MENDELIAN

More info about ROBERTS SYNDROME

Top 5 symptoms//phenotypes associated to Congestive heart failure and Clinodactyly of the 5th finger

Symptoms // Phenotype % cases
Hypertelorism Common - Between 50% and 80% cases
Global developmental delay Common - Between 50% and 80% cases
Brachydactyly Common - Between 50% and 80% cases
Abnormality of cardiovascular system morphology Common - Between 50% and 80% cases
Clinodactyly Common - Between 50% and 80% cases
Mendelian

Accelerate your rare disease diagnosis with us

Learn more

Other less frequent symptoms

Patients with Congestive heart failure and Clinodactyly of the 5th finger. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases


Abnormality of the skeletal system Downslanted palpebral fissures Intellectual disability Short stature Wide nasal bridge Broad forehead Low-set ears Joint hyperflexibility Myopia High palate Growth delay Scoliosis Craniosynostosis Respiratory failure Intellectual disability, mild Micrognathia Seizures Malar flattening Ventricular septal defect Anteverted nares High forehead Depressed nasal bridge Long philtrum Ptosis Abnormal facial shape Strabismus Protruding ear Finger syndactyly Everted lower lip vermilion Corneal opacity Glaucoma Flexion contracture Pain Nystagmus Myocardial infarction Dilatation Delayed eruption of teeth Bicuspid aortic valve Single transverse palmar crease Short palm Inguinal hernia Pectus excavatum Cleft palate Short chin Hearing impairment Abnormality of the dentition Respiratory distress Cryptorchidism Microcephaly Paralysis Dolichocephaly Patent ductus arteriosus Abnormal heart morphology Proptosis

Rare Symptoms - Less than 30% cases


Telecanthus Hypoplasia of dental enamel Coarse facial features Camptodactyly of finger Blepharophimosis Pes planus Hemiparesis Umbilical hernia Hip dislocation Short neck Epicanthus Neoplasm Gait ataxia Sensorineural hearing impairment Short toe Cleft upper lip Wormian bones Thin vermilion border External ear malformation Bowing of the long bones Cataract Respiratory tract infection Short phalanx of finger Facial asymmetry Radial deviation of finger Genu recurvatum Megalocornea Intrauterine growth retardation Full cheeks Arrhythmia Hyperextensible skin Generalized hypotonia Hypoplasia of the maxilla Pulmonic stenosis Short foot Small hand Fever Dyspnea Short nose Short philtrum Preauricular pit Cardiac arrest Underdeveloped supraorbital ridges Short thumb Syndactyly Talipes equinovarus Microphthalmia Double outlet right ventricle Muscle weakness Joint laxity Widely spaced teeth Redundant skin Scaphocephaly Intellectual disability, severe Sparse hair Postnatal growth retardation Aortic aneurysm Toe syndactyly Thick vermilion border Anemia Hypotrichosis Long face Brachycephaly Osteoporosis Persistence of primary teeth Kyphosis Prominent occiput Hernia Hip dysplasia Specific learning disability Finger clinodactyly Short palpebral fissure Coarctation of aorta Premature birth Broad nasal tip Hypodontia Frontal bossing Highly arched eyebrow Macrocephaly Short long bone Cholelithiasis Short mandibular rami Acne Buphthalmos Prominent coccyx Broad clavicles Multiple skeletal anomalies Hyperplasia of the maxilla Broad alveolar ridges Thoracolumbar kyphosis Vacuolated lymphocytes Anterior segment developmental abnormality Concave nasal ridge Flat occiput Beaking of vertebral bodies Abnormally large globe Premature loss of teeth Aseptic necrosis Abnormality of the metacarpal bones Delayed cranial suture closure Flared metaphysis Metatarsus adductus Tricuspid regurgitation Congenital glaucoma Dental malocclusion Osteolysis Antegonial notching of mandible Mandibular prognathia Prominent forehead Motor delay Prominent U wave Hyperkalemia Prominent frontal sinuses Bidirectional ventricular ectopy Prolonged QT interval Agenesis of permanent teeth Osteopenia Periodic hyperkalemic paralysis Long nose Slender long bone Abnormal heart valve morphology Hyperthyroidism Periodic paralysis Delayed eruption of permanent teeth Toe clinodactyly Clinodactyly of the 5th toe Kyphoscoliosis Skeletal dysplasia Gynecomastia Genu valgum Short metatarsal Wide anterior fontanel Gingival overgrowth Thickened skin Interphalangeal joint contracture of finger Mitral valve prolapse Periodic hypokalemic paresis Hirsutism Smooth philtrum Wide mouth High pitched voice Hypokalemia Joint stiffness Abnormality of the pinna Myotonia Camptodactyly Cortical irregularity Deeply set eye 2-3 toe syndactyly Loss of consciousness Serpentine fibula Abnormal toenail morphology Anterior concavity of thoracic vertebrae Knee flexion contracture Proximal placement of thumb Clitoral hypertrophy Radioulnar synostosis Polycystic kidney dysplasia Hypoplasia of the radius Melanoma Hemangioma Sandal gap Opacification of the corneal stroma Bilateral single transverse palmar creases Absent thumb Aortic valve stenosis Blue sclerae Underdeveloped nasal alae Chest pain Falls Prominent nasal bridge Retrognathia Polyhydramnios Posteriorly rotated ears Thrombocytopenia Short femoral neck Aplasia/Hypoplasia of the thumb Broad distal phalanges of all fingers Phocomelia Midface capillary hemangioma Tetraphocomelia Mesomelic arm shortening Progressive flexion contractures Absent earlobe Facial hemangioma Complete duplication of thumb phalanx Aplasia of the ulna Wrist flexion contracture Humeroradial synostosis Long penis Hip contracture Subvalvular aortic stenosis Patellar aplasia Abnormality of the upper limb Fair hair Low hanging columella Capillary hemangioma Upper limb undergrowth Severe intrauterine growth retardation Synostosis of carpal bones Absent radius Malformation of the hepatic ductal plate Incisional hernia Hepatomegaly Limb undergrowth Abnormality of the fingernails Abnormality of dental enamel Hypocalcemia Short ribs Hepatic fibrosis Rhizomelia Omphalocele Abnormality of the metaphysis Fine hair Hypotelorism Microdontia Chronic kidney disease Ectodermal dysplasia Nephropathy High, narrow palate Retinal dystrophy Short distal phalanx of finger Hepatic failure Stage 5 chronic kidney disease Narrow chest Photophobia Renal insufficiency Cutis laxa Cupped ear Renal magnesium wasting Slow-growing hair Broad toe Tubulointerstitial abnormality Short nail Interstitial pneumonitis Thin nail Flattened epiphysis Abnormality of the abdominal wall Abnormal diaphysis morphology Hepatic cysts Sagittal craniosynostosis Ventricular arrhythmia Abnormality of dental morphology Elevated serum creatinine Anodontia Tubulointerstitial nephritis Taurodontia Protuberant abdomen Fibular hypoplasia Short humerus High hypermetropia Short thorax Thoracic hypoplasia Growth abnormality Agenesis of corpus callosum Oligodontia Macrotia Pyloric stenosis Coxa vara Coxa valga Thin skin Arachnodactyly Dilated cardiomyopathy Hypertrophic cardiomyopathy Gastroesophageal reflux Fatigue Telangiectasia of the skin Hypertension Muscular hypotonia Abnormal vertebral segmentation and fusion Abnormality of the cervical spine High anterior hairline Broad foot Shawl scrotum Broad palm Round face Rocker bottom foot Keratoconus Talipes Femoral hernia Alopecia Respiratory insufficiency Failure to thrive Abnormality of the zygomatic bone Abnormal carotid artery morphology Keratoglobus Long palm Median cleft lip and palate Arterial stenosis Prematurely aged appearance Avascular necrosis of the capital femoral epiphysis Abnormal myocardium morphology Myocarditis Esophagitis Aortic dissection Cardiorespiratory arrest Hiatus hernia Pulmonary artery stenosis Aortic root aneurysm Oral cleft Attention deficit hyperactivity disorder Difficulty walking Polycythemia Right ventricular failure Interrupted aortic arch Breathing dysregulation Pulmonary artery atresia Right ventricular hypertrophy Truncus arteriosus Hyperventilation Poor appetite Heart murmur Endocarditis Clubbing Easy fatigability Increased body weight Sinusitis Ventricular hypertrophy Tetralogy of Fallot Cyanosis Abnormal cardiac septum morphology Recurrent respiratory infections Abnormal nasal morphology Overriding aorta Low-set, posteriorly rotated ears Triangular mouth Behavioral abnormality Cognitive impairment Distal/middle symphalangism of 5th finger Mesoaxial foot polydactyly Symphalangism of the 5th finger Muscular ventricular septal defect Parasomnia No permanent dentition Mesoaxial hand polydactyly Short middle phalanx of the 5th finger Pulmonary valve atresia Supernumerary nipple Hand polydactyly Coarse hair Depressed nasal ridge Sleep disturbance Thick eyebrow Polydactyly Absence of the pulmonary valve Tetralogy of Fallot with absent pulmonary valve Pneumonia Conductive hearing impairment Ventricular tachycardia Abnormal palate morphology Neurogenic bladder Congenital nystagmus Bowing of the legs Unilateral renal agenesis Chorioretinal coloboma Relative macrocephaly Genu varum Aplasia/Hypoplasia of the corpus callosum Aortic regurgitation Profound global developmental delay Dental crowding Thick lower lip vermilion Intellectual disability, profound Bilateral sensorineural hearing impairment Progressive visual loss Convex nasal ridge Renal agenesis Esotropia Prominent nose Hypoplasia of teeth Colpocephaly Iris coloboma Bulbous nose Scapular winging Decreased body weight Palpitations Tetraparesis Renal hypoplasia Short metacarpal Syncope Triangular face Inability to walk Tachycardia Short upper lip Thin upper lip vermilion Delayed skeletal maturation Depressivity Ataxia Posterior staphyloma Short 2nd toe Scleral staphyloma Lop ear Lens luxation Microcornea Coloboma Limitation of joint mobility Alopecia of scalp Stiff neck Broad femoral neck Short 1st metacarpal Short hallux Myositis Broad neck Exostoses Ankylosis Basal ganglia calcification Low-grade fever Hamartoma Spinal rigidity Hallux valgus Metaphyseal widening Back pain Sarcoma Aspiration Abnormal vertebral morphology Subcutaneous nodule Overbite Soft tissue sarcoma Mental deterioration Spasticity Intellectual disability, moderate Hydronephrosis Autism Absent speech Atrial septal defect Hypoplasia of the corpus callosum Ventriculomegaly Optic atrophy Visual impairment Aplasia/Hypoplasia of the phalanges of the hallux Synostosis of joints 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 Osteochondroma Premature separation of centromeric heterochromatin



If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like Melanoma and Respiratory tract infection, related diseases and genetic alterations Myopia and Peripheral demyelination, related diseases and genetic alterations

Need help with a diagnosis?

Learn more about how to achieve it with Mendelian


Learn more