Cognitive impairment, and Myocardial infarction

Diseases related with Cognitive impairment and Myocardial infarction

In the following list you will find some of the most common rare diseases related to Cognitive impairment and Myocardial infarction that can help you solving undiagnosed cases.


Top matches:

Medium match CARDIOMYOPATHY, DILATED, 1V; CMD1V


Related symptoms:

  • Cardiomyopathy
  • Congestive heart failure
  • Dementia
  • Dilated cardiomyopathy
  • Syncope


SOURCES: OMIM MESH MENDELIAN

More info about CARDIOMYOPATHY, DILATED, 1V; CMD1V

Medium match ALZHEIMER DISEASE 2; AD2


A degenerative disease of the brain characterized by the insidious onset of dementia. Impairment of memory, judgment, attention span, and problem solving skills are followed by severe apraxia and a global loss of cognitive abilities. The condition primarily occurs after age 60, and is marked pathologically by severe cortical atrophy and the triad of senile plaques, neurofibrillary tangles, and neuropil threads. [HPO:probinson]

ALZHEIMER DISEASE 2; AD2 Is also known as alzheimer disease associated with apoe4|alzheimer disease 2, late-onset

Related symptoms:

  • Hypertension
  • Dementia
  • Diabetes mellitus
  • Stroke
  • Parkinsonism


SOURCES: OMIM MESH MENDELIAN

More info about ALZHEIMER DISEASE 2; AD2

Medium match HOMOCYSTINURIA DUE TO METHYLENE TETRAHYDROFOLATE REDUCTASE DEFICIENCY


Homocystinuria due to methylene tetrahydrofolate reductase (MTHFR) deficiency is a metabolic disorder characterised by neurological manifestations.

HOMOCYSTINURIA DUE TO METHYLENE TETRAHYDROFOLATE REDUCTASE DEFICIENCY Is also known as methylenetetrahydrofolate reductase deficiency|mthfr deficiency|methylene tetrahydrofolate reductase deficiency

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Generalized hypotonia
  • Microcephaly


SOURCES: OMIM ORPHANET MENDELIAN

More info about HOMOCYSTINURIA DUE TO METHYLENE TETRAHYDROFOLATE REDUCTASE DEFICIENCY

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Other less relevant matches:

Medium match SNEDDON SYNDROME


Sneddon's syndrome (SS) is a rare non-inflammatory thrombotic vasculopathy characterized by the combination of cerebrovascular disease with livedo racemosa.

SNEDDON SYNDROME Is also known as livedo reticularis-cerebrovascular accident syndrome|livedo racemosa-cerebrovascular accident syndrome|livedo reticularis and cerebrovascular accidents|ehrmann-sneddon syndrome

Related symptoms:

  • Seizures
  • Muscle weakness
  • Pain
  • Visual impairment
  • Motor delay


SOURCES: OMIM MESH ORPHANET MENDELIAN

More info about SNEDDON SYNDROME

Medium match ALKAPTONURIA


Alkaptonuria is a metabolic disease characterized by the accumulation of homogentisic acid (HGA) and its oxidized product, benzoquinone acetic acid (BQA), in various tissues (e.g. cartilage, connective tissue) and body fluids (urine, sweat), causing urine to darken when exposed to air as well as grey-blue coloration of the sclera and ear helix (ochronosis), and a disabling joint disease involving both the axial and peripheral joints (ochronotic arthropathy).

ALKAPTONURIA Is also known as homogentisic acid oxidase deficiency|hereditary ochronosis

Related symptoms:

  • Pain
  • Cognitive impairment
  • Hypertension
  • Kyphosis
  • Abnormality of metabolism/homeostasis


SOURCES: ORPHANET OMIM MESH MENDELIAN

More info about ALKAPTONURIA

Medium match LYMPHANGIOLEIOMYOMATOSIS


Lymphangioleiomyomatosis (LAM) is a multiple cystic lung disease characterized by progressive cystic destruction of the lung and lymphatic abnormalities, frequently associated with renal angiomyolipomas (AMLs). LAM occurs either sporadically or as a manifestation of tuberous sclerosis complex (TSC).

LYMPHANGIOLEIOMYOMATOSIS Is also known as lam|lymphangiomyomatosis

Related symptoms:

  • Seizures
  • Pain
  • Cognitive impairment
  • Fever
  • Optic atrophy


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about LYMPHANGIOLEIOMYOMATOSIS

Medium match CADASIL


CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy) is a hereditary cerebrovascular disorder characterized by mid-adult onset of recurrent subcortical ischemic stroke and cognitive impairment progressing to dementia in addition to migraines with aura and mood disturbances seen in about a third of patients.

CADASIL Is also known as dementia, hereditary multi-infarct type|cadasil|cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy|casil|hereditary multi-infarct dementia

Related symptoms:

  • Seizures
  • Hearing impairment
  • Ataxia
  • Sensorineural hearing impairment
  • Muscle weakness


SOURCES: OMIM ORPHANET MENDELIAN

More info about CADASIL

Medium match CEREBROTENDINOUS XANTHOMATOSIS


Cerebrotendinous xanthomatosis (CTX) is an anomaly of bile acid synthesis (see this term) characterized by neonatal cholestasis, childhood-onset cataract, adolescent to young adult-onset tendon xanthomata, and brain xanthomata with adult-onset neurologic dysfunction.

CEREBROTENDINOUS XANTHOMATOSIS Is also known as cerebral cholesterinosis|sterol 27-hydroxylase deficiency|ctx

Related symptoms:

  • Intellectual disability
  • Seizures
  • Ataxia
  • Nystagmus
  • Muscle weakness


SOURCES: MESH OMIM ORPHANET MENDELIAN

More info about CEREBROTENDINOUS XANTHOMATOSIS

Medium match WOODHOUSE-SAKATI SYNDROME


Woodhouse-Sakati syndrome is a multisystemic disorder characterized by hypogonadism, alopecia, diabetes mellitus, intellectual deficit and extrapyramidal signs with choreoathetoid movements and dystonia.

WOODHOUSE-SAKATI SYNDROME Is also known as hypogonadism, alopecia, diabetes mellitus, mental retardation, deafness, and extrapyramidal syndrome|extrapyramidal disorder, progressive, with primary hypogonadism, mental retardation, and alopecia|diabetes-hypogonadism-deafness-intellectual disability s

Related symptoms:

  • Intellectual disability
  • Seizures
  • Hearing impairment
  • Scoliosis
  • Hypertelorism


SOURCES: ORPHANET OMIM MESH MENDELIAN

More info about WOODHOUSE-SAKATI SYNDROME

Medium match NOONAN SYNDROME WITH MULTIPLE LENTIGINES


Noonan syndrome with multiple lentigines (NSML), previously known as LEOPARD syndrome, is a rare multisystem genetic disorder characterized by lentigines, hypertrophic cardiomyopathy, short stature, pectus deformity, and dysmorphic facial features.

NOONAN SYNDROME WITH MULTIPLE LENTIGINES Is also known as leopard syndrome|cardiomyopathic lentiginosis|familial multiple lentigines syndrome

Related symptoms:

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


SOURCES: ORPHANET OMIM MENDELIAN

More info about NOONAN SYNDROME WITH MULTIPLE LENTIGINES

Top 5 symptoms//phenotypes associated to Cognitive impairment and Myocardial infarction

Symptoms // Phenotype % cases
Seizures Common - Between 50% and 80% cases
Dementia Uncommon - Between 30% and 50% cases
Behavioral abnormality Uncommon - Between 30% and 50% cases
Intellectual disability, mild Uncommon - Between 30% and 50% cases
Stroke Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

Patients with Cognitive impairment and Myocardial infarction. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases


Muscle weakness Hypertension Peripheral neuropathy Dysarthria Pain Intellectual disability Spasticity Gait disturbance Tremor Ataxia Scoliosis Abnormality of extrapyramidal motor function Hyperreflexia Mental deterioration Sensorineural hearing impairment Developmental regression Hearing impairment Memory impairment Atherosclerosis Abnormality of the eye Hallucinations

Rare Symptoms - Less than 30% cases


Sensory neuropathy Aphasia Delusions Babinski sign Joint dislocation Transient ischemic attack Joint stiffness Headache Visual impairment Abnormality of the ear Facial palsy Hypertelorism Confusion Vertigo EEG abnormality Fever Migraine Hemiparesis Personality changes Pallor Progressive neurologic deterioration Cerebral ischemia Psychosis Depressivity Abnormality of skin pigmentation Abnormality of metabolism/homeostasis Pseudobulbar paralysis Bundle branch block Diabetes mellitus Parkinsonism Triangular face Amaurosis fugax Global developmental delay Generalized hypotonia Diarrhea Dystonia Delayed speech and language development Delayed puberty Coma Truncal ataxia Melanoma Attention deficit hyperactivity disorder Hemiplegia Nephrolithiasis Abnormality of vision Encephalopathy Cerebral atrophy EMG: axonal abnormality Abnormality of cholesterol metabolism Palatal myoclonus Abnormality of the dentate nucleus EEG with generalized slow activity Frontal lobe dementia Cardiomyopathy Tuberous xanthoma Arthrogryposis multiplex congenita Fine hair Bilateral sensorineural hearing impairment Dehydration Amenorrhea Decreased testicular size Dental malocclusion Prominent nose Polyneuropathy Abnormality of movement Hypotrichosis Prominent nasal bridge Abnormality of central somatosensory evoked potentials Sparse hair Protruding ear Camptodactyly High forehead Micropenis Hypogonadism Alopecia Frontal bossing Downslanted palpebral fissures High palate Hypothyroidism Hypercholesterolemia Tendon xanthomatosis Myoclonus Congenital cataract Abnormality of the cerebral white matter Spastic paraplegia Neurological speech impairment Abnormal pyramidal sign Aggressive behavior Jaundice Osteoporosis Cerebellar atrophy Paraplegia Respiratory insufficiency Cataract Nystagmus Subdural hemorrhage Scintillating scotoma Nonarteritic anterior ischemic optic neuropathy Recurrent subcortical infarcts Abulia Malabsorption Neurodegeneration Juvenile cataract Abnormality of the periventricular white matter Giant cell hepatitis Xanthelasma Myelopathy Decreased HDL cholesterol concentration Precocious atherosclerosis Xanthomatosis Angina pectoris Frontotemporal dementia Agitation Abnormal cerebellum morphology Cholelithiasis Chronic diarrhea Cholestasis Intention tremor Optic disc pallor Hepatitis Cerebral calcification Progressive cerebellar ataxia Primary amenorrhea Growth delay Sparse scalp hair Subcutaneous nodule Bilateral cryptorchidism Melanocytic nevus Abnormality of the voice Myelodysplasia Hyperextensible skin Spina bifida occulta Scapular winging Cafe-au-lait spot Left ventricular hypertrophy Abnormality of the face Decreased fertility Abnormality of the genital system Mitral valve prolapse Tetralogy of Fallot Specific learning disability Webbed neck Nevus Thick vermilion border Joint hyperflexibility Pulmonic stenosis External genital hypoplasia Atrioventricular canal defect Abnormality of the kidney Abnormal mitral valve morphology Hypoplasia of the ovary Abnormal pulmonary valve morphology Abnormal endocardium morphology Multiple lentigines Excessive wrinkled skin Abnormality of the pulmonary artery Abnormal localization of kidney Abnormal aortic valve morphology Shield chest Aplasia/Hypoplasia of the abdominal wall musculature Freckling Redundant neck skin Wolff-Parkinson-White syndrome Right ventricular hypertrophy Premature skin wrinkling Sprengel anomaly Severe sensorineural hearing impairment Curly hair Neuroblastoma Multiple cafe-au-lait spots Pectus carinatum Low-set, posteriorly rotated ears Choreoathetosis Insulin-resistant diabetes mellitus Decreased serum insulin-like growth factor 1 Streak ovary Increased thyroid-stimulating hormone level Abnormal spermatogenesis Abnormal T-wave Decreased serum estradiol Decreased serum testosterone level Anodontia Heart block Autoimmune thrombocytopenia Hypoplasia of the fallopian tube Hypoplasia of the uterus Aplasia/Hypoplasia of the eyebrow Flat occiput Sparse eyebrow Premature ovarian insufficiency Hyperlipidemia Purpura Hypogonadotrophic hypogonadism Hypergonadotropic hypogonadism Progressive extrapyramidal movement disorder Progressive alopecia Hypertrophic cardiomyopathy Abnormality of cardiovascular system morphology Neonatal hypotonia Mandibular prognathia Hyperkeratosis Brachycephaly Posteriorly rotated ears Delayed skeletal maturation Arrhythmia Pectus excavatum Hypospadias Dilatation Short stature Short neck Intrauterine growth retardation Wide nasal bridge Depressed nasal bridge Low-set ears Ptosis Cryptorchidism Muscular hypotonia Retinal arteriolar tortuosity Subcortical dementia Inability to walk Focal sensory seizure Lupus anticoagulant Aminoaciduria Abnormality of the nail Osteoarthritis Blue sclerae Aciduria Arthritis Arthralgia Kyphosis Antiphospholipid antibody positivity Growth abnormality Vascular skin abnormality Thromboembolic stroke Arterial stenosis Hemianopia Facial paralysis Peripheral arterial stenosis Arteriovenous malformation Acrocyanosis Reduced bone mineral density Abnormality of the urinary system Atrophic scars Hearing abnormality Calcification of cartilage Intervertebral disc degeneration Mitral valve calcification Aortic valve calcification Dark urine Chronic pain Low back pain Abnormality of the nose Ankylosis Back pain Joint swelling Irregular hyperpigmentation Arthropathy Abnormal joint morphology Abnormal heart valve morphology Hyperparathyroidism Vertebral fusion Aortic aneurysm Thrombocytosis Visual field defect Prostatitis Agnosia Apnea Abnormality of the nervous system Proximal muscle weakness Hyperactivity Intellectual disability, severe Hypoplasia of the corpus callosum Failure to thrive Microcephaly Long-tract signs Lethargy Neurofibrillary tangles Alzheimer disease Apraxia Myocardial fibrosis Abnormal EKG Abnormality of the cardiovascular system Syncope Dilated cardiomyopathy Severe global developmental delay Limb muscle weakness Cutis marmorata Motor delay Heart murmur Intracranial hemorrhage Systemic lupus erythematosus Vasculitis Chorea Nephropathy Paralysis Myalgia Hyperhomocystinemia Paresthesia Homocystinuria Thromboembolism Coronary artery atherosclerosis Poor suck Incoordination Paraparesis Hypsarrhythmia Epileptic encephalopathy Waddling gait Cartilage destruction Coronary artery calcification Diffuse leukoencephalopathy Lower limb muscle weakness Peripheral demyelination Abnormality of the skin Urinary incontinence Brain atrophy Tetraplegia Congestive heart failure Nausea Dysmetria Abnormality of eye movement Tetraparesis Generalized tonic-clonic seizures Hypoglycemia Cerebral cortical atrophy Elevated serum creatine phosphokinase Visual loss Hypertonia Vomiting Myopathy Bradykinesia Recurrent pneumonia Chylopericardium Optic neuropathy Subcutaneous hemorrhage Mania Perseveration Abnormality of nervous system morphology Migraine with aura Stroke-like episode Varicose veins Abnormality of visual evoked potentials Impaired pain sensation Spastic tetraparesis Amyloidosis Bulbar palsy Scotoma Cerebral hemorrhage Apathy Abnormal electroretinogram Leukoencephalopathy Cranial nerve paralysis Shock Dysphagia Pulmonary lymphangiomyomatosis Tendon rupture Recurrent respiratory infections Chest pain Ascites Hematuria Lymphadenopathy Cough Dyspnea Respiratory failure Abdominal pain Hydrocephalus Abnormal lung morphology Respiratory distress Fatigue Optic atrophy Ochronosis Pigmentation of the sclera Tendonitis Intervertebral disk calcification Thickened Achilles tendon Gastrointestinal hemorrhage Lymphedema Cystic lung disease Bronchiolitis Ungual fibroma Retinal hamartoma Renal angiomyolipoma Bronchiolitis obliterans Shagreen patch Abnormal urinary color Abnormality of the lymphatic system Chylothorax Pneumothorax Nephroblastoma Abnormality of female internal genitalia Atelectasis Renal neoplasm Multiple renal cysts Pulmonary infiltrates Hemoptysis Macule Restrictive ventilatory defect Emphysema Numerous nevi



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