Congestive heart failure, and Aggressive behavior

Diseases related with Congestive heart failure and Aggressive behavior

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


Top matches:

High match MEND SYNDROME


MEND syndrome is a rare, genetic, syndromic, sterol biosynthesis disorder affecting males characterized by skin manifestations, including collodion membrane, ichthyosis, and patchy hypopigmentary lesions, associated with severe neurological involvement (e.g. intellectual disability, delayed psychomotor development, seizures, hydrocephalus, cerebellar/corpus callosum hypoplasia, Dandy-Walker malformation, hypotonia) and craniofacial dysmorphism (large anterior fontanelle, telecanthus, hypertelorism, microphthalmia, prominent nasal bridge, low-set ears, micrognathia, cleft palate). 2,3 toe syndactyly, polydactyly, and kyphosis, as well as ophthalmic, cardiac and urogenital anomalies may also be associated.

MEND SYNDROME Is also known as male ebp disorder with neurologic defects|male ebp disorder with neurological defects

Related symptoms:

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


SOURCES: ORPHANET OMIM MENDELIAN

More info about MEND SYNDROME

High match GAUCHER DISEASE TYPE 3


Gaucher disease type 3 is the subacute neurological form of Gaucher disease (GD; see this term) characterized by progressive encephalopathy and associated with the systemic manifestations (organomegaly, bone involvement, cytopenia) of GD type 1 (see this term).

GAUCHER DISEASE TYPE 3 Is also known as chronic neuronopathic gaucher disease|cerebral juvenile and adult form of gaucher disease|gaucher disease, subacute neuronopathic type

Related symptoms:

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


SOURCES: ORPHANET MENDELIAN

More info about GAUCHER DISEASE TYPE 3

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Other less relevant matches:

Medium 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 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 ACQUIRED IDIOPATHIC SIDEROBLASTIC ANEMIA


Acquired idiopathic sideroblastic anaemia is one of a group of disorders known as the myelodysplastic syndromes (MDS) characterised by ineffective haemopoiesis affecting one or more blood cell lineages (myeloid, erythroid or megakaryocytic) leading to peripheral blood cytopenias and an increased risk of developing leukaemia. Acquired idiopathic sideroblastic anaemia is now more commonly referred to as refractory anaemia with ringed sideroblasts or the acronym RARS.

ACQUIRED IDIOPATHIC SIDEROBLASTIC ANEMIA Is also known as rars|primary acquired sideroblastic anemia|refractory anemia with ringed sideroblasts|aisa

Related symptoms:

  • Pain
  • Anemia
  • Fatigue
  • Respiratory distress
  • Congestive heart failure


SOURCES: OMIM ORPHANET MENDELIAN

More info about ACQUIRED IDIOPATHIC SIDEROBLASTIC ANEMIA

Low match ACYL-COA DEHYDROGENASE, VERY LONG-CHAIN, DEFICIENCY OF; ACADVLD


Inborn errors of mitochondrial fatty acid beta-oxidation include medium-chain acyl-CoA dehydrogenase deficiency (OMIM ), short-chain acyl-CoA dehydrogenase deficiency (OMIM ), and very long-chain acyl-CoA dehydrogenase deficiency.VLCAD deficiency can be classified clinically into 3 forms: a severe early-onset form with high incidence of cardiomyopathy and high mortality; an intermediate form with childhood onset, usually with hypoketotic hypoglycemia and more favorable outcome; and an adult-onset, myopathic form with isolated skeletal muscle involvement, rhabdomyolysis, and myoglobinuria after exercise or fasting (Andresen et al., 1999).Patients reported with long-chain acyl-CoA dehydrogenase (LCAD) deficiency before VLCAD deficiency was defined were later found to have VLCAD deficiency (Strauss et al., 1995; Roe and Ding, 2001).

ACYL-COA DEHYDROGENASE, VERY LONG-CHAIN, DEFICIENCY OF; ACADVLD Is also known as vlcad deficiency

Related symptoms:

  • Generalized hypotonia
  • Muscle weakness
  • Muscular hypotonia
  • Pain
  • Hepatomegaly


SOURCES: OMIM MENDELIAN

More info about ACYL-COA DEHYDROGENASE, VERY LONG-CHAIN, DEFICIENCY OF; ACADVLD

Low match SYSTEMIC PRIMARY CARNITINE DEFICIENCY


Systemic primary carnitine deficiency (SPCD) is a potentially lethal disorder of fatty acid oxidation characterized classically by early childhood onset cardiomyopathy often with weakness and hypotonia, failure to thrive and recurrent hypoglycemic hypoketotic seizures and/or coma.

SYSTEMIC PRIMARY CARNITINE DEFICIENCY Is also known as cud|carnitine uptake deficiency|carnitine transporter defect|systemic carnitine deficiency|deficiency of plasma-membrane carnitine transporter|scd|carnitine deficiency, primary|carnitine deficiency, systemic, due to defect in renal reabsorption of carniti

Related symptoms:

  • Seizures
  • Generalized hypotonia
  • Failure to thrive
  • Muscle weakness
  • Muscular hypotonia


SOURCES: ORPHANET MESH OMIM MENDELIAN

More info about SYSTEMIC PRIMARY CARNITINE DEFICIENCY

Low match GLYCOGEN STORAGE DISEASE DUE TO LAMP-2 DEFICIENCY


Glycogen storage disease due to LAMP-2 (Lysosomal-Associated Membrane Protein 2) deficiency is a lysosomal glycogen storage disease characterised by severe cardiomyopathy and variable degrees of muscle weakness, frequently associated with intellectual deficit.

GLYCOGEN STORAGE DISEASE DUE TO LAMP-2 DEFICIENCY Is also known as vacuolar cardiomyopathy and myopathy, x-linked|antopol disease|gsd due to lamp-2 deficiency|lysosomal glycogen storage disease without acid maltase deficiency, formerly|glycogenosis due to lamp-2 deficiency|gsd2b, formerly|gsd iib, formerly|glycogen stora

Related symptoms:

  • Intellectual disability
  • Global developmental delay
  • Muscle weakness
  • Pain
  • Cognitive impairment


SOURCES: MESH ORPHANET OMIM MENDELIAN

More info about GLYCOGEN STORAGE DISEASE DUE TO LAMP-2 DEFICIENCY

Low 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

Top 5 symptoms//phenotypes associated to Congestive heart failure and Aggressive behavior

Symptoms // Phenotype % cases
Arrhythmia Common - Between 50% and 80% cases
Fatigue Uncommon - Between 30% and 50% cases
Hepatomegaly Uncommon - Between 30% and 50% cases
Intellectual disability Uncommon - Between 30% and 50% cases
Seizures Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases


Global developmental delay Cardiomyopathy Irritability Generalized hypotonia Vomiting Encephalopathy Dilated cardiomyopathy Short stature Cardiomegaly Hydrocephalus Scoliosis Failure to thrive Cerebral cortical atrophy Muscular hypotonia Edema Pain Muscle weakness Gait disturbance Hypertonia Hypertrophic cardiomyopathy Thick vermilion border Hyperactivity Growth delay Strabismus Ataxia Myopia Kyphosis Depressivity Ventriculomegaly Abdominal pain Hepatosplenomegaly Mental deterioration Decreased body weight Abnormal heart valve morphology Abnormal myocardium morphology Hepatic steatosis Decreased liver function Elevated serum creatine phosphokinase Myopathy Respiratory tract infection Delayed skeletal maturation Feeding difficulties in infancy Dysphagia Cognitive impairment Skeletal muscle atrophy Cataract High palate

Rare Symptoms - Less than 30% cases


Hyperammonemia Left ventricular hypertrophy Abnormal retinal morphology Exercise intolerance Skeletal myopathy Abnormality of the sternum Progressive visual loss Dental malocclusion Ventricular hypertrophy Cardiorespiratory arrest Fever Interstitial pulmonary abnormality Rigidity Decreased plasma carnitine Joint hypermobility Hypoketotic hypoglycemia Pericardial effusion Brachydactyly Hyperextensibility of the finger joints Sleep apnea Redundant skin Lymphadenopathy Hematuria Abdominal distention Delayed gross motor development Abnormal bleeding Aplasia/Hypoplasia of the corpus callosum Myocardial infarction Cutis laxa Abnormality of the skeletal system Narrow palate Oculomotor apraxia Hypoalbuminemia Open mouth Hypertelorism Hearing impairment Feeding difficulties Dementia Macrotia Respiratory distress Neurological speech impairment Headache Autism Pectus carinatum Scarring Coarse facial features Inguinal hernia Erythema Dysarthria Palpitations Telecanthus Abnormality of the eye Chest pain Respiratory insufficiency Hypoglycemia Ptosis Downslanted palpebral fissures Abnormal aortic valve morphology Cardiac arrest Depressed nasal bridge Epicanthus Macrocephaly Optic atrophy Frontal bossing Pectus excavatum Anteverted nares Cerebral atrophy Atrial septal defect Intellectual disability, severe Behavioral abnormality Coma Lethargy Mitral regurgitation Respiratory insufficiency due to muscle weakness Abnormal tricuspid valve morphology Wide nose Diarrhea Supranuclear gaze palsy Anemia Nystagmus Proteinuria Broad hallux Neurodevelopmental delay Self-injurious behavior Narrow forehead Single transverse palmar crease Micrognathia Bulbous nose Thrombocytopenia Long face Ichthyosis Sensorineural hearing impairment Abnormal cardiac septum morphology Low-set, posteriorly rotated ears Polyhydramnios Posteriorly rotated ears Abnormality of the gastrointestinal tract Cryptorchidism Low-set ears Hypoplasia of the corpus callosum Ventricular septal defect Splenomegaly Pallor Abnormal mitral valve morphology Psychosis Recurrent respiratory infections Scaling skin Osteopenia Loss of consciousness Mandibular prognathia Bifid sternum Uterine prolapse Abnormal facial shape Peripheral neuropathy Intellectual disability, mild Frontal balding Kyphoscoliosis Abnormality of dental morphology Thick nasal septum Pes planus Hyperlordosis Protruding ear Wide mouth Severe global developmental delay Morphological abnormality of the gastrointestinal tract Aplasia/Hypoplasia of the cerebellum Lumbar kyphosis Cerebellar vermis hypoplasia Abnormality of the nasal alae Prominent supraorbital ridges Tachycardia Abnormal form of the vertebral bodies Thick lower lip vermilion Abnormality of retinal pigmentation Patchy alopecia Wide anterior fontanel Inappropriate crying Abnormality of the auditory canal Abnormality of the hair Multiple palmar creases Coxa valga Thick eyebrow Eyelid fasciculation Multiple plantar creases Oral aversion Widely spaced teeth Microcephaly Cutaneous T-cell lymphoma Schizophrenia Coarse hair Optic nerve dysplasia Drumstick terminal phalanges Joint hyperflexibility Retinoschisis Progressive spasticity Soft skin Hypoplastic fingernail Cutis marmorata Abnormality of the hairline Hyperkeratosis pilaris Tetraplegia Tongue thrusting Generalized ichthyosis Acrocyanosis Laryngeal cleft Severe sensorineural hearing impairment Restrictive cardiomyopathy Spinal canal stenosis Short metacarpal Anteriorly placed anus Atonic seizures Abnormality of neuronal migration Thickened calvaria Functional abnormality of the gastrointestinal tract Broad palm Abnormality of digit Emphysema Abnormality of the optic disc Abnormal location of ears Short distal phalanx of finger Hypodontia Pseudoepiphyses of the metacarpals Stooped posture Cataplexy Everted lower lip vermilion Highly arched eyebrow Tapered finger Delayed eruption of teeth Hyperconvex fingernails Broad finger Narrow iliac wings Thick nasal alae Craniofacial hyperostosis Large hands Hypoplasia of the maxilla Premature loss of primary teeth Rectal prolapse Puberty and gonadal disorders Anterior creases of earlobe Advanced eruption of teeth Hypoplasia of the frontal lobes Myelopathy Delayed closure of the anterior fontanelle Abnormal diaphysis morphology Hepatocellular necrosis Microcytic anemia Glycogen accumulation in muscle fiber lysosomes Cranial nerve paralysis Conjunctivitis Vasculitis Meningitis Cholestasis Hepatitis Migraine Nausea and vomiting Skin rash Arthritis Jaundice Arthralgia Dilatation Increased cerebral lipofuscin Hyponatremia Suicidal ideation Macular hypopigmentation Left ventricular systolic dysfunction Myocardial necrosis Ventricular preexcitation Impaired myocardial contractility Exercise-induced muscle cramps Retinal pigment epithelial mottling Muscle flaccidity Autophagic vacuoles Myofibrillar myopathy Myocardial fibrosis Wolff-Parkinson-White syndrome Ischemic stroke Leukocytosis Hypokinesia Glossitis Aseptic leukocyturia Strawberry tongue Double outlet right ventricle with subpulmonary ventricular septal defect without pulmonary stenosis Abnormal emotion/affect behavior Pyuria Arthralgia/arthritis Abnormality of nail color Coronary artery aneurysm Cervical lymphadenopathy CSF pleocytosis Conjunctival hyperemia Abnormal pericardium morphology Arteritis Abnormal oral mucosa morphology Coronary artery atherosclerosis Cholecystitis Ascending tubular aorta aneurysm Synovitis Cheilitis Elevated C-reactive protein level Inflammatory abnormality of the eye Recurrent pharyngitis Allergy Myocarditis Tubulointerstitial nephritis Aortic root aneurysm Acute kidney injury Pericarditis Elevated erythrocyte sedimentation rate Reduced ejection fraction Generalized amyotrophy Increased serum ferritin Drowsiness Easy fatigability Bradycardia Clumsiness Confusion Elevated hepatic transaminase Exercise-induced rhabdomyolysis Increased nuchal translucency Exercise-induced myoglobinuria Nonketotic hypoglycemia Dicarboxylic aciduria Respiratory arrest Exercise-induced myalgia Myoglobinuria Rhabdomyolysis Neck muscle weakness Tachypnea Muscle stiffness Sudden cardiac death Muscle cramps Metabolic acidosis Autistic behavior Myalgia Acidosis Refractory sideroblastic anemia Crackles Hypochromic anemia Abnormal glucose tolerance Sideroblastic anemia Decreased mean corpuscular volume Decreased muscle mass Ketonuria Back pain Proximal muscle weakness Abnormal electroretinogram Ventricular arrhythmia EMG: myopathic abnormalities Cone/cone-rod dystrophy Ventricular tachycardia Hyperlipidemia Atrial fibrillation Pigmentary retinopathy Distal sensory impairment Distal amyotrophy Limb muscle weakness Retinopathy Abnormality of the liver Reduced visual acuity Excessive daytime somnolence Pes cavus Visual loss Hypertension Visual impairment Decreased carnitine level in liver Irregular respiration Reduced muscle carnitine level Impaired gluconeogenesis Reye syndrome-like episodes Acute encephalopathy Generalized tonic-clonic seizures with focal onset Fasting hypoglycemia Endocardial fibroelastosis Recurrent hypoglycemia Endocarditis Relative macrocephaly Sparse or absent eyelashes Lymphopenia Petechiae Opisthotonus Increased antibody level in blood Pulmonary fibrosis Menorrhagia Clubbing Abnormality of the thorax Portal hypertension Cholelithiasis Increased susceptibility to fractures Leukopenia Osteolysis Increased bone mineral density Bone pain Lower limb hyperreflexia Hydrops fetalis Progressive neurologic deterioration Intention tremor Epistaxis Pulmonary arterial hypertension Pancytopenia Cyanosis Syncope Progressive cerebellar ataxia Generalized myoclonic seizures Ascites Neurodegeneration Cirrhosis Restrictive ventilatory defect Bulbar palsy Delayed puberty Spontaneous hematomas Neoplasm Sleep myoclonus Abnormality of the acoustic reflex Abnormality of ion homeostasis Cardiac valve calcification Horizontal supranuclear gaze palsy Hematological neoplasm Decreased beta-glucocerebrosidase protein and activity Erlenmeyer flask deformity of the femurs Orthopnea Mitral valve calcification Abnormal saccadic eye movements Aortic valve calcification Abnormal thrombosis Exertional dyspnea Generalized osteosclerosis Astrocytosis Protein-losing enteropathy Restrictive deficit on pulmonary function testing Avascular necrosis of the capital femoral epiphysis Abnormality of the spleen Multiple myeloma Hypercoagulability Vertebral compression fractures Slow saccadic eye movements Thoracic kyphosis Hepatocellular carcinoma Aseptic necrosis Abnormality of eye movement Malabsorption Short neck Disinhibition Prominent nasal bridge Muscular hypotonia of the trunk Deeply set eye Skeletal dysplasia Polydactyly Agenesis of corpus callosum Midface retrusion Syndactyly Cleft palate Semantic dementia Bulimia Perseveration Primitive reflex Pulmonary edema Smooth philtrum Abnormal lower motor neuron morphology Frontotemporal dementia Insomnia Global brain atrophy Agitation Amyotrophic lateral sclerosis Emotional lability Personality changes Apathy Stereotypy Neuronal loss in central nervous system Chorea Babinski sign Toe syndactyly Hypopigmentation of the skin Ophthalmoplegia Otosclerosis Generalized tonic-clonic seizures Corneal opacity Abnormal pyramidal sign Difficulty walking Dyspnea Osteoporosis Myoclonus Dystonia Tremor Olivopontocerebellar hypoplasia Hypoplastic aortic arch Spotty hypopigmentation Long neck Overlapping fingers Esotropia Narrow nose Epiphyseal stippling Long fingers Ectopic kidney Overlapping toe 2-3 toe syndactyly Overfolded helix Sacral dimple Microretrognathia Narrow palpebral fissure Aortic valve stenosis Dandy-Walker malformation Wide intermamillary distance Delayed speech and language development Blindness Multiple lentigines Heart murmur Curly hair Biparietal narrowing Multiple cafe-au-lait spots Long palpebral fissure Infantile spasms Neurofibromas Aplasia/Hypoplasia of the eyebrow Hydroureter Malnutrition Open bite Large for gestational age Absent eyebrow Obsessive-compulsive behavior Chronic otitis media Submucous cleft hard palate Cubitus valgus Melanocytic nevus Ectropion Pleural effusion Sparse eyebrow Bilateral ptosis Failure to thrive in infancy Brittle hair Deep philtrum Hyperextensible skin Poor suck Spasticity Abnormality of vision Generalized hyperpigmentation Anal stenosis Optic nerve hypoplasia Dystrophic fingernails Cavernous hemangioma Abnormality of hair texture Excessive wrinkled skin Abnormality of the pulmonary artery Subvalvular aortic stenosis Thickened helices Slow-growing hair Gastrointestinal dysmotility Deep palmar crease Abnormality of refraction Delayed CNS myelination Abnormality of the testis Abnormality of the optic nerve Abnormal hair pattern Underdeveloped supraorbital ridges Thick upper lip vermilion Woolly hair Short attention span Abnormality of the ulna Premature skin wrinkling Hypoplasia of the zygomatic bone Absent eyelashes Enlarged kidney Arnold-Chiari type I malformation Abnormal eyelash morphology Alopecia of scalp Atopic dermatitis Poor appetite Palmoplantar hyperkeratosis Abnormality of the genitourinary system Abnormality of the dentition Gastroesophageal reflux Pulmonic stenosis Hypotrichosis Hypermetropia Abnormality of the cerebral white matter Dolichocephaly Nail dystrophy Pruritus Leukemia Sparse hair Abnormality of the kidney Hydronephrosis EEG abnormality Umbilical hernia High forehead Astigmatism Proptosis Hyperkeratosis Hyperhidrosis Prominent forehead Alopecia Constipation Clinodactyly of the 5th finger Abnormal heart morphology Hernia Abnormality of cardiovascular system morphology Malar flattening Long philtrum Short nose Genu valgum Dry skin Hemangioma Coarctation of aorta Abnormal palate morphology Sparse eyelashes Abnormality of the nail Aspiration Cerebral visual impairment Hyperpigmentation of the skin Lymphedema Cafe-au-lait spot Thickened skin Inflammatory abnormality of the skin Hemiparesis Fine hair Low posterior hairline Abnormality of the cardiovascular system Peripheral axonal neuropathy Growth hormone deficiency Webbed neck Premature birth Intestinal malrotation Vesicoureteral reflux Nevus Full cheeks Palmoplantar keratoderma Sleep disturbance High, narrow palate Retinal dystrophy Bruising susceptibility Falls Abnormality of skin pigmentation Abnormal gallbladder morphology



If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like Frontal bossing and Polydactyly, related diseases and genetic alterations Abnormality of the skeletal system and Proptosis, related diseases and genetic alterations

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