Congestive heart failure, and Delayed eruption of teeth

Diseases related with Congestive heart failure and Delayed eruption of teeth

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


Top matches:

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

Medium match MUCOPOLYSACCHARIDOSIS, TYPE II; MPS2


Mucopolysaccharidosis II is a rare X-linked recessive disorder caused by deficiency of the lysosomal enzyme iduronate sulfatase, leading to progressive accumulation of glycosaminoglucans in nearly all cell types, tissues, and organs. Patients with MPS II excrete excessive amounts of chondroitin sulfate B (dermatan sulfate) and heparitin sulfate (heparan sulfate) in the urine (McKusick, 1972; Wraith et al., 2008).

MUCOPOLYSACCHARIDOSIS, TYPE II; MPS2 Is also known as hunter syndrome|sulfoiduronate sulfatase deficiency|sids deficiency|mps ii|ids deficiency|iduronate 2-sulfatase deficiency

Related symptoms:

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


SOURCES: OMIM MENDELIAN

More info about MUCOPOLYSACCHARIDOSIS, TYPE II; MPS2

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Other less relevant matches:

Medium 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

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 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

Low match HENNEKAM SYNDROME


Hennekam syndrome is characterised by the association of lymphoedema, intestinal lymphangiectasia, intellectual deficit and facial dysmorphism.

HENNEKAM SYNDROME Is also known as lymphedema-lymphangiectasia-intellectual disability syndrome|lymphatic dysplasia, generalized|hennekam lymphangiectasia-lymphedema syndrome

Related symptoms:

  • Intellectual disability
  • Seizures
  • Hearing impairment
  • Scoliosis
  • Growth delay


SOURCES: ORPHANET OMIM MENDELIAN

More info about HENNEKAM SYNDROME

Low 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

Low match HUTCHINSON-GILFORD PROGERIA SYNDROME


Hutchinson-Gilford progeria syndrome is a rare, fatal, autosomal dominant and premature aging disease, beginning in childhood and characterized by growth reduction, failure to thrive, a typical facial appearance (prominent forehead, protuberant eyes, thin nose with a beaked tip, thin lips, micrognathia and protruding ears) and distinct dermatologic features (generalized alopecia, aged-looking skin, sclerotic and dimpled skin over the abdomen and extremities, prominent cutaneous vasculature, dyspigmentation, nail hypoplasia and loss of subcutaneous fat).

HUTCHINSON-GILFORD PROGERIA SYNDROME Is also known as progeria|hgps

Related symptoms:

  • Intellectual disability
  • Short stature
  • Hearing impairment
  • Scoliosis
  • Growth delay


SOURCES: OMIM ORPHANET MENDELIAN

More info about HUTCHINSON-GILFORD PROGERIA SYNDROME

Top 5 symptoms//phenotypes associated to Congestive heart failure and Delayed eruption of teeth

Symptoms // Phenotype % cases
Scoliosis Common - Between 50% and 80% cases
Intellectual disability Common - Between 50% and 80% cases
Global developmental delay Common - Between 50% and 80% cases
Hearing impairment Common - Between 50% and 80% cases
Seizures Common - Between 50% and 80% cases
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Other less frequent symptoms

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

Common Symptoms - More than 50% cases


Short stature

Uncommon Symptoms - Between 30% and 50% cases


Broad forehead

Common Symptoms - More than 50% cases


Wide nasal bridge

Uncommon Symptoms - Between 30% and 50% cases


Hypertelorism

Common Symptoms - More than 50% cases


Umbilical hernia

Uncommon Symptoms - Between 30% and 50% cases


Abnormal facial shape Abnormality of the skeletal system Cognitive impairment Strabismus Downslanted palpebral fissures Pectus excavatum Hypodontia Coarse facial features Intellectual disability, severe Macrocephaly Kyphosis Cardiomyopathy Growth delay Abnormality of the dentition Thick vermilion border Camptodactyly of finger Short palm Inguinal hernia Sensorineural hearing impairment Clinodactyly of the 5th finger Low-set ears Depressed nasal bridge Anteverted nares High palate Brachydactyly Malar flattening Protruding ear Cataract Single transverse palmar crease Gingival overgrowth Muscular hypotonia Mandibular prognathia Abnormality of dental morphology Attention deficit hyperactivity disorder Finger syndactyly Thick lower lip vermilion Spina bifida occulta Small hand Short foot Osteolysis Osteopenia Hypoplasia of the maxilla Hirsutism Decreased body weight Delayed skeletal maturation Micrognathia Hepatomegaly Corneal opacity Splenomegaly Hepatosplenomegaly Wide mouth Macrotia Flexion contracture Everted lower lip vermilion Thick eyebrow Short philtrum Abnormality of cardiovascular system morphology Intellectual disability, mild Syndactyly Ventricular septal defect Epicanthus Ptosis

Rare Symptoms - Less than 30% cases


Generalized hypotonia Hypertension Toe syndactyly Dilatation Myelopathy Dyspnea Polyhydramnios Retinoschisis Narrow palate Camptodactyly Scaphocephaly Abnormal heart valve morphology Sleep apnea Joint hypermobility Widely spaced teeth Short distal phalanx of finger Intellectual disability, progressive Kyphoscoliosis Highly arched eyebrow Rectal prolapse Abnormality of retinal pigmentation Short neck Joint stiffness Polydactyly Craniosynostosis Microcephaly Wide anterior fontanel Thickened skin Dilated cardiomyopathy Myopia Coxa valga Dental malocclusion Short nose Long philtrum Thin vermilion border Abnormality of the hair Smooth philtrum High forehead Muscle weakness Skeletal muscle atrophy Pain Clinodactyly Cerebral cortical atrophy Patent ductus arteriosus Alopecia Respiratory distress Gait disturbance Hypertrichosis Bulbous nose Proptosis Tetraparesis External ear malformation Supernumerary nipple High pitched voice Visual impairment Narrow chest Conductive hearing impairment Persistence of primary teeth Loss of consciousness Hyperextensibility of the finger joints Short phalanx of finger Genu recurvatum Megalocornea Diarrhea Short chin Broad palm Narrow mouth Midface retrusion Oral cleft Oligodontia Joint hyperflexibility Cleft palate Cryptorchidism Growth abnormality Pes planus Hydrocephalus Hypoplastic fingernail Coarse hair Hernia Tetraplegia Macroglossia Pericardial effusion Short metacarpal Prominent forehead Broad nasal tip Glaucoma Metaphyseal widening Microtia Coarctation of aorta Thin bony cortex Prolonged QT interval Intellectual disability, profound Talipes equinovarus Bicuspid aortic valve Osteoporosis Abnormality of digit Cutis marmorata Mitral regurgitation Large hands Progressive spasticity Cutis laxa Aplasia/Hypoplasia of the corpus callosum Broad hallux Thickened calvaria Schizophrenia Atonic seizures Anteriorly placed anus Aplasia/Hypoplasia of the cerebellum Severe sensorineural hearing impairment Spinal canal stenosis Emphysema Redundant skin Self-injurious behavior Abnormality of neuronal migration Soft skin Prominent supraorbital ridges Abnormal form of the vertebral bodies Periorbital edema Open mouth Hypoalbuminemia Hypoproteinemia Sparse axillary hair Nonimmune hydrops fetalis Arteriovenous malformation Hypoplastic iliac wing Edema of the lower limbs Polysplenia Coronal craniosynostosis Palpebral edema Increased number of teeth Cutaneous finger syndactyly Ectopic kidney Pleural effusion Pyloric stenosis Protein-losing enteropathy Reduced number of teeth Cutaneous syndactyly Abnormal intestine morphology Horseshoe kidney Hypocalcemia Bilateral single transverse palmar creases Joint contracture of the hand Lymphopenia Hydrops fetalis Lymphedema Pachygyria Decreased antibody level in blood Vesicoureteral reflux Generalized edema Restrictive cardiomyopathy Cerebellar vermis hypoplasia Frontal bossing Psychosis Tapered finger Wide nose Severe global developmental delay Neurological speech impairment Pectus carinatum Hyperlordosis Feeding difficulties in infancy Mental deterioration Telecanthus Hypertonia Hypoplasia of the corpus callosum Ventriculomegaly Optic atrophy Chylothorax Peripheral neuropathy Pleural lymphangiectasia Pericardial lymphangiectasia Thyroid lymphangiectasia Mild postnatal growth retardation Benign neoplasm of the central nervous system Conical incisor Severe hydrops fetalis Pulmonary lymphangiectasia Lymphangioma Erysipelas Intestinal lymphangiectasia Abnormal oral mucosa morphology Primary hypothyroidism Acrocyanosis Cardiomegaly Abnormal mitral valve morphology Thrombocytosis Small face Generalized osteoporosis Lack of skin elasticity Angina pectoris Prominent superficial veins Osteolytic defects of the phalanges of the hand Ovoid vertebral bodies Hyperphosphatemia Down-sloping shoulders Fragile nails Transient ischemic attack Absent eyelashes Abnormal EKG Alopecia of scalp Precocious atherosclerosis Short clavicles Renal cell carcinoma Hypoplastic nipples Keratoconjunctivitis sicca Thin ribs Scleroderma Lipoatrophy Exertional dyspnea Premature graying of hair Multiple joint contractures Heart murmur Abnormality of the thorax Premature ovarian insufficiency Hyperinsulinemia Aplasia/Hypoplasia of the earlobes Enlarged joints Intracranial hemorrhage Mitral valve calcification Arteriosclerosis of small cerebral arteries Regional abnormality of skin Abnormal trabecular bone morphology Insulin-resistant diabetes mellitus at puberty Absence of pubertal development Carotid artery stenosis Narrow nasal tip Bilateral coxa valga Craniofacial disproportion Old-aged sensorineural hearing impairment Reticulated skin pigmentation Hypoplastic facial bones Prominent scalp veins Bird-like facies Parietal bossing Decreased serum estradiol Widely patent fontanelles and sutures Intermittent claudication Corneal arcus Sinus tachycardia Decreased testosterone in males Premature coronary artery atherosclerosis Thin nail Absence of subcutaneous fat Hip pain Aplastic clavicle Narrow nasal ridge Arteriosclerosis Carcinoid tumor Prolonged prothrombin time Lipodystrophy Nasal speech Craniofacial hyperostosis Bifid sternum Hypermetropia Hip dislocation Stroke Sparse hair Hypertrophic cardiomyopathy Carcinoma Hypogonadism Dementia Failure to thrive Neoplasm Drumstick terminal phalanges Abnormality of the nasal alae Thick nasal septum Uterine prolapse Carious teeth Lumbar kyphosis Pseudoepiphyses of the metacarpals Stooped posture Cataplexy Hyperconvex fingernails Abnormal tricuspid valve morphology Broad finger Narrow iliac wings Thick nasal alae Abnormal diaphysis morphology Premature loss of primary teeth Advanced eruption of teeth Abnormal aortic valve morphology Delayed closure of the anterior fontanelle Hypotrichosis Delayed puberty Dermal atrophy Dental crowding Relative macrocephaly Hypercholesterolemia Acanthosis nigricans Hyperlipidemia Atherosclerosis Aminoaciduria Hypogonadotrophic hypogonadism Hypergonadotropic hypogonadism Increased bone mineral density Aspiration Aortic valve stenosis Sparse and thin eyebrow Insulin resistance Hypohidrosis Left ventricular hypertrophy Infertility Broad-based gait Thin skin Osteoarthritis Hypertriglyceridemia Myocardial infarction Flat face Abnormality of the cardiovascular system Cyanosis Convex nasal ridge Nail dysplasia Growth hormone deficiency Limitation of joint mobility Chest pain Hepatic steatosis Ascites Tricuspid regurgitation Lymphadenopathy Blue sclerae Abnormality of immune system physiology Telangiectasia of the skin Hemiplegia/hemiparesis Keratitis Encephalitis Eosinophilia Hypopigmented skin patches Abnormality of the fingernails Abnormality of dental enamel Abnormality of the nail Skin ulcer Pulmonary arterial hypertension Uveitis Abnormal blistering of the skin Retinal detachment Abnormality of skin pigmentation Skin rash Erythema Hyperkeratosis Hyperhidrosis Microphthalmia Spasticity Dermatan sulfate excretion in urine Tracheobronchomalacia Irregular hyperpigmentation Hearing abnormality Urinary glycosaminoglycan excretion Ataxia Tachycardia Facial asymmetry Pulmonic stenosis Blepharophimosis Paralysis Joint laxity Thin upper lip vermilion Gait ataxia Arrhythmia Depressivity Fever Retinal vascular proliferation Abnormal toenail morphology Broad nail Abnormal hand morphology Ridged fingernail Abnormal chorioretinal morphology Absent hand Retinal hemorrhage Asymmetric growth Supernumerary ribs Deviation of finger Cerebral ischemia Verrucae Dystrophic toenail Cervical cord compression Heparan sulfate excretion in urine Triangular face Symphalangism of the 5th finger High anterior hairline Broad foot Shawl scrotum Hyperextensible skin Round face Cleft upper lip Talipes Low-set, posteriorly rotated ears Behavioral abnormality Distal/middle symphalangism of 5th finger Mesoaxial foot polydactyly Muscular ventricular septal defect Abnormal vertebral segmentation and fusion Parasomnia No permanent dentition Mesoaxial hand polydactyly Triangular mouth Short middle phalanx of the 5th finger Prominent occiput Hand polydactyly Finger clinodactyly Depressed nasal ridge Premature birth Sleep disturbance Abnormality of the cervical spine Pes cavus Retinal fold Hoarse voice Intestinal pseudo-obstruction Dysostosis multiplex Obstructive sleep apnea Papilledema Mild short stature Incoordination Corneal dystrophy Aortic regurgitation Spastic tetraparesis Exercise intolerance Elbow flexion contracture Split hand Severe short stature Recurrent otitis media Progressive neurologic deterioration Spastic tetraplegia Pigmentary retinopathy Asthma Postural instability Neurodegeneration Abnormality of the cerebral white matter Dolichocephaly Retinopathy Apnea Rod-cone dystrophy Inability to walk Syncope Abnormality of the foot Anterior concavity of thoracic vertebrae Hemangioma Accelerated skeletal maturation Hemivertebrae Generalized hirsutism Nephrolithiasis Small nail Bilateral sensorineural hearing impairment Overgrowth Synophrys Congenital cataract Posteriorly rotated ears Cortical irregularity Anonychia Serpentine fibula Prominent coccyx Broad clavicles Multiple skeletal anomalies Hyperplasia of the maxilla Broad alveolar ridges Thoracolumbar kyphosis Vacuolated lymphocytes Anterior segment developmental abnormality Buphthalmos Concave nasal ridge Large for gestational age Aortic root aneurysm Abnormally large globe Respiratory insufficiency Malabsorption Respiratory tract infection Abnormality of the kidney Intellectual disability, moderate Hydronephrosis Retrognathia Hypothyroidism Hyperactivity Recurrent respiratory infections Edema Atrial septal defect Mesiodens Protruding tongue Short distal phalanx of toe Prominent eyelashes Aortic arch aneurysm Everted upper lip vermilion Generalized hypertrichosis Biliary atresia Cavernous hemangioma Gingival fibromatosis Long penis Colpocephaly Dystrophic fingernails Broad ribs Beaking of vertebral bodies Double outlet right ventricle Specific learning disability Hyperkalemia Periodic hyperkalemic paralysis Short mandibular rami Periodic hypokalemic paresis Clinodactyly of the 5th toe Toe clinodactyly Delayed eruption of permanent teeth Periodic paralysis Hyperthyroidism Slender long bone Long nose Agenesis of permanent teeth 2-3 toe syndactyly Bidirectional ventricular ectopy Preauricular pit Myotonia Hypokalemia Short metatarsal Ventricular arrhythmia Ventricular tachycardia Scapular winging Cardiac arrest Hypoplasia of dental enamel Palpitations Short palpebral fissure Renal hypoplasia Antegonial notching of mandible Prominent frontal sinuses Premature loss of teeth Gynecomastia Aseptic necrosis Congenital glaucoma Delayed cranial suture closure Flared metaphysis Metatarsus adductus Flat occiput Acne Cholelithiasis Short long bone Abnormality of the metacarpal bones Wormian bones Bowing of the long bones Prominent U wave Interphalangeal joint contracture of finger Mitral valve prolapse Hip dysplasia Full cheeks Genu valgum Abnormality of the pinna Deeply set eye Skeletal dysplasia Respiratory failure Brachycephaly Abnormal heart morphology Motor delay Tapering pointed ends of distal finger phalanges



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