Congestive heart failure, and Psychosis

Diseases related with Congestive heart failure and Psychosis

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

Top matches:

Spinocerebellar ataxia type 7 (SCA7), currently the only known form of autosomal dominant cerebellar ataxia type 2 (ADCA2; see this term), is a neurodegenerative disorder characterized by progressive ataxia, motor system abnormalities, dysarthria, dysphagia and retinal degeneration leading to progressive blindness.

SPINOCEREBELLAR ATAXIA TYPE 7 Is also known as ataxia with pigmentary retinopathy|sca7|cerebellar syndrome-pigmentary maculopathy syndrome

Related symptoms:

  • Global developmental delay
  • Ataxia
  • Nystagmus
  • Failure to thrive
  • Muscle weakness


SOURCES: ORPHANET MENDELIAN

More info about SPINOCEREBELLAR ATAXIA TYPE 7

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

Short-chain acyl-CoA dehydrogenase (SCAD) deficiency is a very rare inborn error of mitochondrial fatty acid oxidation characterized by variable manifestations ranging from asymptomatic individuals (in most cases) to those with failure to thrive, hypotonia, seizures, developmental delay and progressive myopathy.

SHORT CHAIN ACYL-COA DEHYDROGENASE DEFICIENCY Is also known as scad deficiency|scadh deficiency|acads deficiency|lipid-storage myopathy secondary to short-chain acyl-coa dehydrogenase deficiency|scadd

Related symptoms:

  • Seizures
  • Global developmental delay
  • Generalized hypotonia
  • Microcephaly
  • Scoliosis


SOURCES: OMIM MESH ORPHANET MENDELIAN

More info about SHORT CHAIN ACYL-COA DEHYDROGENASE DEFICIENCY

Other less relevant matches:

The proximal 16p11.2 microdeletion syndrome is a chromosomal anomaly characterized by developmental and language delays, mild intellectual disability, social impairments (autism spectrum disorders), mild variable dysmorphism and predisposition to obesity.

PROXIMAL 16P11.2 MICRODELETION SYNDROME Is also known as proximal del(16)(p11.2)|proximal monosomy 16p11.2

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Microcephaly
  • Scoliosis


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about PROXIMAL 16P11.2 MICRODELETION SYNDROME

Combined methylmalonic aciduria (MMA) and homocystinuria is a genetically heterogeneous disorder of cobalamin (cbl; vitamin B12) metabolism. The defect causes decreased levels of the coenzymes adenosylcobalamin (AdoCbl) and methylcobalamin (MeCbl), which results in decreased activity of the respective enzymes methylmalonyl-CoA mutase (MUT ) and methyltetrahydrofolate:homocysteine methyltransferase, also known as methionine synthase (MTR ). Different forms of the disorder have been classified according to complementation groups of cells in vitro: cblC, cblD (OMIM ), cblF (OMIM ), and cblJ (OMIM ).Isolated methylmalonic acidurias have also been classified by complementation groups: MMA 'mut' (OMIM ) is caused by mutation in the MUT gene on chromosome 6p21; MMA cblA (OMIM ) is caused by mutation in the MMAA gene (OMIM ) on 4q31; and MMA cblB (OMIM ) is caused by mutation in the MMAB gene (OMIM ) on 12q24.Methylmalonic aciduria and homocystinuria, cblC type, is the most common inborn error of vitamin B12 (cobalamin) metabolism, with about 250 known cases (Lerner-Ellis et al., 2006). Affected individuals may have developmental, hematologic, neurologic, metabolic, ophthalmologic, and dermatologic clinical findings. Although considered a disease of infancy or childhood, some individuals develop symptoms in adulthood (Rosenblatt et al., 1997).

METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC Is also known as vitamin b12 metabolic defect with combined deficiency of methylmalonyl-coa mutase and homocysteine:methyltetrahydrofolate methyltransferase|methylmalonic aciduria and homocystinuria, vitamin b12-responsive|methylmalonic acidemia and homocystinuria, cblc t

Related symptoms:

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


SOURCES: ORPHANET OMIM MENDELIAN

More info about METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC

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

Prader-Willi syndrome is characterized by diminished fetal activity, obesity, muscular hypotonia, mental retardation, short stature, hypogonadotropic hypogonadism, and small hands and feet. It can be considered to be an autosomal dominant disorder and is caused by deletion or disruption of a gene or several genes on the proximal long arm of the paternal chromosome 15 or maternal uniparental disomy 15, because the gene(s) on the maternal chromosome(s) 15 are virtually inactive through imprinting. Horsthemke and Wagstaff (2008) provided a detailed review of the mechanisms of imprinting of the Prader-Willi/Angelman syndrome (OMIM ) region.See also the chromosome 15q11-q13 duplication syndrome (OMIM ), which shows overlapping clinical features.

PRADER-WILLI SYNDROME; PWS Is also known as prader-labhart-willi syndrome

Related symptoms:

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


SOURCES: OMIM MENDELIAN

More info about PRADER-WILLI SYNDROME; PWS

Medium match MELAS

MELAS (Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke) syndrome is a rare progressive multisystemic disorder characterized by encephalomyopathy, lactic acidosis, and stroke-like episodes. Other features include endocrinopathy, heart disease, diabetes, hearing loss, and neurological and psychiatric manifestations.

MELAS Is also known as mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes|melas syndrome|mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes

Related symptoms:

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


SOURCES: ORPHANET OMIM MESH MENDELIAN

More info about MELAS

Familial glucocorticoid deficiency-5 is characterized by resistance to adrenocorticotropic hormone (ACTH) and isolated glucocorticoid deficiency, with typical biochemical findings of low serum cortisol levels and high plasma ACTH. Patients commonly present with hyperpigmentation (Prasad et al., 2014).For a discussion of genetic heterogeneity of familial glucocorticoid deficiency, see GCCD1 (OMIM ).

Related symptoms:

  • Ventricular septal defect
  • Congestive heart failure
  • Truncus arteriosus


SOURCES: OMIM MENDELIAN

More info about GLUCOCORTICOID DEFICIENCY 5; GCCD5

Familial dyskinesia and facial myokymia is a rare paroxysmal movement disorder, with childhood or adolescent onset, characterized by paroxysmal choreiform, dystonic, and myoclonic movements involving the limbs (mostly distal upper limbs), neck and/or face, which can progressively increase in both frequency and severity until they become nearly constant. Patients may also present with delayed motor milestones, perioral and periorbital dyskinesias, dysarthria, hypotonia, and weakness.

FAMILIAL DYSKINESIA AND FACIAL MYOKYMIA Is also known as fdfm

Related symptoms:

  • Intellectual disability
  • Generalized hypotonia
  • Motor delay
  • Hyperreflexia
  • Dysarthria


SOURCES: ORPHANET MESH OMIM MENDELIAN

More info about FAMILIAL DYSKINESIA AND FACIAL MYOKYMIA

Top 5 symptoms//phenotypes associated to Congestive heart failure and Psychosis

Symptoms // Phenotype % cases
Global developmental delay Common - Between 50% and 80% cases
Intellectual disability Common - Between 50% and 80% cases
Seizures Common - Between 50% and 80% cases
Muscular hypotonia Common - Between 50% and 80% cases
Growth delay Common - Between 50% and 80% cases

Other less frequent symptoms

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

Common Symptoms - More than 50% cases

Muscle weakness

Uncommon Symptoms - Between 30% and 50% cases

Feeding difficulties Failure to thrive Cardiomyopathy Motor delay Hypertension Cognitive impairment Generalized hypotonia Microcephaly Mental deterioration Myopathy Respiratory insufficiency Nystagmus Scoliosis Hyperactivity Dilated cardiomyopathy Cataract Hypertonia Feeding difficulties in infancy Ventriculomegaly Optic atrophy Hearing impairment Weight loss Cerebral cortical atrophy Lethargy Delayed speech and language development Intellectual disability, severe Acidosis Tremor Abnormal facial shape Ataxia Strabismus Tapered finger Ptosis Attention deficit hyperactivity disorder Intrauterine growth retardation Abnormality of the pinna Vomiting Macrotia Autism Intellectual disability, mild Hypertelorism Pigmentary retinopathy Skeletal muscle atrophy Depressivity Ophthalmoplegia Abnormality of retinal pigmentation Gait disturbance Photophobia Reduced visual acuity Respiratory distress Visual loss Kyphosis Myopia Visual impairment Pain Short stature Dysarthria Hyperreflexia

Rare Symptoms - Less than 30% cases

Anorexia Short nose Pulmonary embolism Acrocyanosis Short neck Hemiplegia Dilatation Delayed skeletal maturation Behavioral abnormality Anxiety Cor pulmonale Myelopathy Peripheral neuropathy Anteverted nares Inguinal hernia Epicanthus Depressed nasal bridge High palate Involuntary movements Macrocephaly Low-set ears Sensorineural hearing impairment Cryptorchidism Adrenal insufficiency Obesity EEG abnormality Micropenis Gait ataxia Neurological speech impairment Hydrocephalus Renal insufficiency External ophthalmoplegia Dementia Nephropathy Myoclonus Dystonia Joint hypermobility Difficulty walking Proteinuria Congenital cataract Malabsorption Confusion Anemia Decreased body weight Pulmonary arterial hypertension Memory impairment Gastroesophageal reflux Protruding ear Paresthesia Wide mouth Smooth philtrum Small hand Abnormality of neuronal migration Psychotic episodes Large hands Aplasia/Hypoplasia of the cerebellum Narrow palpebral fissure Schizophrenia Bilateral ptosis Sleep apnea Progressive external ophthalmoplegia Micrognathia Decreased fetal movement Hepatomegaly Pruritus Hip dysplasia Orofacial dyskinesia Polymicrogyria Retinopathy Hemeralopia Diabetes mellitus Hypogonadism Fever Hypogonadotrophic hypogonadism Cardiac arrest Hypertrophic cardiomyopathy Fatigue Wolff-Parkinson-White syndrome Carious teeth Arrhythmia Abnormality of the dentition Elevated serum creatine phosphokinase Osteoporosis Abnormality of the liver Cardiorespiratory arrest Delayed puberty Hyporeflexia Ophthalmoparesis Specific learning disability Type II diabetes mellitus Amenorrhea Metabolic acidosis Left ventricular hypertrophy Abnormality of the cardiovascular system Exercise intolerance Dysphagia Blindness Cerebellar atrophy Hepatic steatosis Cerebral atrophy Atrial fibrillation Neonatal hypotonia Respiratory tract infection Dysmetria Ventricular hypertrophy Hypoglycemia Encephalopathy Apnea Sensory impairment Aciduria Macular degeneration Stroke Cone/cone-rod dystrophy Hypothyroidism Abdominal pain Rod-cone dystrophy Dyspnea Generalized tonic-clonic seizures Jaundice Gastrointestinal hemorrhage Generalized myoclonic seizures Abnormal cerebellum morphology Muscle cramps Full cheeks Postural instability Coma Polyneuropathy Hirsutism Nausea Lactic acidosis Peripheral axonal neuropathy Febrile seizures Vertigo Ichthyosis Anal atresia Nausea and vomiting Arthrogryposis multiplex congenita Esotropia Nyctalopia Erythema Developmental regression Growth hormone deficiency Myalgia Narrow forehead Almond-shaped palpebral fissure Cerebellar hypoplasia Hyperinsulinemia Scrotal hypoplasia Oligomenorrhea Overweight Infantile muscular hypotonia Poor suck Central hypotonia Abnormality of lipid metabolism Iris hypopigmentation Nasal speech Failure to thrive in infancy Hypoventilation Hypopigmentation of hair Precocious puberty Radial deviation of finger Spontaneous abortion Emotional lability Inflammation of the large intestine Glucose intolerance Striae distensae Albinism Impaired pain sensation Skeletal muscle hypertrophy Migraine Myeloid leukemia Narrow nasal bridge Polyphagia External genital hypoplasia Truncal obesity Decreased muscle mass Bicuspid aortic valve Hypoplasia of the fovea Constipation Primary amenorrhea Areflexia Headache Diarrhea Acromicria Poor gross motor coordination Oligohydramnios Hypopnea Narrow palm Hypoplastic labia minora Central adrenal insufficiency Temperature instability Triangular mouth Cutaneous photosensitivity Disseminated intravascular coagulation Increased body weight Erysipelas Frontal upsweep of hair Clitoral hypoplasia Clumsiness Insulin resistance Anteverted ears Bradycardia Poor fine motor coordination Aortic valve stenosis Abdominal obesity Generalized hypopigmentation Hypothermia Ocular albinism Chromosome breakage Sudden cardiac death Overlapping toe Increased serum lactate Proximal tubulopathy Amaurosis fugax Gastroparesis Spontaneous hematomas Leber optic atrophy Persistence of primary teeth Writer's cramp Muscle fiber atrophy Psychomotor deterioration Dysesthesia Motor polyneuropathy Episodic vomiting Abnormality of the renal tubule Hemianopia Ileus Abnormality of peripheral nerve conduction Abnormal nerve conduction velocity Cerebral ischemia Facial diplegia Aortic dissection Renal tubular dysfunction Tubulointerstitial nephritis Visual hallucinations Increased CSF lactate Reduced consciousness/confusion Retinal pigment epithelial atrophy Gait imbalance Anterior hypopituitarism Stroke-like episode Seborrheic dermatitis Left ventricular failure Speech apraxia Auditory hallucinations Renal Fanconi syndrome Transient ischemic attack Dyskinesia Morphological abnormality of the inner ear Prominent ear helix Ventricular septal defect Truncus arteriosus Muscular hypotonia of the trunk Abnormality of movement Chorea Bilateral intracranial calcifications Choreoathetosis Delayed gross motor development Resting tremor Limb hypertonia Myokymia Paroxysmal dyskinesia Morphological abnormality of the vestibule of the inner ear Episodic quadriplegia Tubulointerstitial abnormality Edema of the dorsum of hands Abnormality of the cerebellar vermis Crohn's disease Abnormal macular morphology Spotty hypopigmentation Paronychia Abnormal mitochondrial morphology Cochlear malformation Abnormality of acid-base homeostasis Progressive night blindness Cochlear degeneration Abnormal mitochondrial shape Paralytic ileus Abnormal cochlea morphology Homonymous hemianopia Delusions Posterior subcapsular cataract Cerebral calcification Reduced tendon reflexes Aortic aneurysm Hypercalciuria Decreased nerve conduction velocity Cachexia Atrioventricular block Chronic kidney disease Growth abnormality Easy fatigability Hyperkinesis Goiter Mutism Hypopigmented skin patches Ischemic stroke Ragged-red muscle fibers Pancreatitis Hyponatremia Gingival overgrowth Generalized-onset seizure Bilateral sensorineural hearing impairment Nephrotic syndrome Status epilepticus Hemiparesis Hypertrichosis Hallucinations Purpura Cerebral visual impairment Clonus Truncal ataxia EMG abnormality Generalized hirsutism Type I diabetes mellitus Abnormality of mitochondrial metabolism Personality changes Mitochondrial myopathy Atopic dermatitis Rhabdomyolysis Thyroiditis Abnormality of immune system physiology Primary adrenal insufficiency Distal arthrogryposis Drowsiness Hashimoto thyroiditis Basal ganglia calcification Abnormality of visual evoked potentials Neonatal hypoglycemia Vitiligo Xerostomia Heart block Hypoparathyroidism Hyperthyroidism Glomerulopathy Intestinal obstruction Aphasia Bifid scrotum Mask-like facies Hemiplegia/hemiparesis Focal segmental glomerulosclerosis Hypopigmentation of the skin Bundle branch block Vestibular dysfunction Progressive sensorineural hearing impairment Dysphasia Hyperkalemia Visual field defect Prolonged QT interval Multiple lipomas Vertebral fusion Sepsis Coarse hair Sleep disturbance Hemivertebrae Arnold-Chiari type I malformation Severe combined immunodeficiency Syringomyelia Long nose Combined immunodeficiency Unilateral renal agenesis Anophthalmia Language impairment Hand polydactyly Pyloric stenosis Aortic regurgitation Microretrognathia Pointed chin Multiple renal cysts Short toe Congenital diaphragmatic hernia Renal agenesis Underdeveloped nasal alae Renal cyst Flat face Talipes Broad forehead Coloboma Blepharophimosis Autistic behavior Deeply set eye Polydactyly Severe intrauterine growth retardation Missing ribs Hernia Hemolytic anemia Thromboembolism Disproportionate tall stature Apathy Ectopia lentis Slurred speech Atherosclerosis Recurrent urinary tract infections Broad-based gait Pancytopenia Abnormality of extrapyramidal motor function Urinary incontinence Neutropenia Hematuria Long face Hydrocele testis Abnormality of skin pigmentation Retinal degeneration Unsteady gait Lower limb muscle weakness Hip dislocation Arthritis High forehead Thrombocytopenia Absent nasal bridge Widely-spaced maxillary central incisors Chorioretinitis Pulmonary artery atresia Optic nerve coloboma Posteriorly rotated ears Midface retrusion Methylmalonic aciduria Palpitations Abnormality of the gastrointestinal tract Hypokinesia Abnormal retinal morphology Generalized amyotrophy Neurodevelopmental delay Back pain Abnormal electroretinogram Ventricular arrhythmia EMG: myopathic abnormalities Respiratory insufficiency due to muscle weakness Ventricular tachycardia Hyperlipidemia Decreased liver function Cardiomegaly Myocardial fibrosis Progressive visual loss Chest pain Distal sensory impairment Distal amyotrophy Limb muscle weakness Scarring Abnormality of the eye Proximal muscle weakness Pes cavus Abnormal fundus morphology Restless legs Dysdiadochokinesis Babinski sign Reduced ejection fraction Myofibrillar myopathy Recurrent infections Abnormality of the cerebral white matter Microphthalmia Immunodeficiency Malar flattening Atrial septal defect Wide nasal bridge Cleft palate Hypoglycemic encephalopathy Ethylmalonic aciduria Episodic metabolic acidosis Nonketotic hypoglycemia U-Shaped upper lip vermilion Decreased plasma carnitine Organic aciduria Facial palsy Skeletal myopathy Flexion contracture Glycogen accumulation in muscle fiber lysosomes Increased cerebral lipofuscin 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 Megaloblastic anemia Homocystinuria Short foot Abnormal mitral valve morphology Abnormal tricuspid valve morphology Broad finger Narrow iliac wings Thick nasal alae Abnormal diaphysis morphology Premature loss of primary teeth Rectal prolapse Hyperextensibility of the finger joints Advanced eruption of teeth Abnormal aortic valve morphology Delayed closure of the anterior fontanelle Craniofacial hyperostosis Restrictive cardiomyopathy Cataplexy Hypoplastic fingernail Soft skin Severe sensorineural hearing impairment Spinal canal stenosis Anteriorly placed anus Atonic seizures Thickened calvaria Broad palm Abnormality of digit Progressive spasticity Broad hallux Loss of consciousness Emphysema Hyperconvex fingernails Stooped posture Abnormality of dental morphology Upslanted palpebral fissure Downturned corners of mouth Short palm Arachnodactyly Infertility Genu valgum Hypermetropia Dolichocephaly Leukemia Abnormality of the nervous system Thin upper lip vermilion Osteopenia Narrow mouth Respiratory failure Prominent forehead Pseudoepiphyses of the metacarpals Recurrent respiratory infections Clinodactyly Syndactyly Edema Talipes equinovarus Neoplasm Drumstick terminal phalanges Abnormality of the nasal alae Thick nasal septum Bifid sternum Uterine prolapse Lumbar kyphosis Retinoschisis Cutis marmorata Self-injurious behavior Gastritis Hypomethioninemia Coarse facial features Kyphoscoliosis Mandibular prognathia Pectus excavatum Hypoplasia of the corpus callosum Abnormality of the skeletal system Frontal bossing Downslanted palpebral fissures Brachydactyly Thyroglossal cyst Cystathioninemia Diffuse hepatic steatosis Decreased methylmalonyl-CoA mutase activity Cystathioninuria Telecanthus Vitamin B12 deficiency Decreased methionine synthase activity Decreased adenosylcobalamin Hyperhomocystinemia Decreased methylcobalamin Urogenital fistula Delirium Abnormality of macular pigmentation Chronic hemolytic anemia Methylmalonic acidemia Atrophy of the spinal cord Hemolytic-uremic syndrome Right ventricular failure Pes planus Hyperlordosis Prominent supraorbital ridges Dental malocclusion Redundant skin Aplasia/Hypoplasia of the corpus callosum Widely spaced teeth Cutis laxa Narrow palate Coxa valga Abnormality of the hair Wide anterior fontanel Mitral regurgitation Abnormal form of the vertebral bodies Open mouth Thick lower lip vermilion Cerebellar vermis hypoplasia Short metacarpal Pectus carinatum Tetraplegia Hypoplasia of the maxilla Hypodontia Delayed eruption of teeth Single transverse palmar crease Highly arched eyebrow Everted lower lip vermilion Thick vermilion border Wide nose Short distal phalanx of finger Thick eyebrow Joint hyperflexibility Severe global developmental delay Facial myokymia


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