|
Acute Febrile Encephalopathy
agenesis of corpus callosum, cardiac, ocular, and genital syndrome
Athabaskan brainstem dysgenesis syndrome
autoimmune cardiomyopathy
Beta-Ureidopropionase Deficiency
Central Auditory Diseases +
central nervous system origin vertigo
CEREBELLAR ATAXIA, BRAIN ABNORMALITIES, AND CARDIAC CONDUCTION DEFECTS
cerebrovascular disease +
chronic atrial and intestinal dysrhythmia
complex cortical dysplasia with other brain malformations +
Congenital Cerebral Granulomas
congenital disorder of deglycosylation 2
congenital heart disease +
congestive heart failure +
disease of mental health +
Encephalopathy due to Defective Mitochondrial and Peroxisomal Fission +
ENCEPHALOPATHY, ACUTE TRANSIENT
ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), 8
ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), 10
ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, 9
ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3
ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND SPASTICITY
GM1 gangliosidosis type 1
heart conduction disease +
heterophyiasis A parasitic helminthiasis infectious disease that involves intestinal infection by the parasite of the genus Heterophyes. The symptoms are diarrhea and colicky abdominal pain. Migration of the eggs to the heart, results in fatal myocardial and valvular damage. Brain can also be infected. (DO)
hypertensive heart disease
immunoglobulin light chain amyloidosis
infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly
INTELLECTUAL DEVELOPMENTAL DISORDER WITH PAROXYSMAL DYSKINESIA OR SEIZURES
intracranial hypertension +
Keratosis Follicularis, Dwarfism, and Cerebral Atrophy
Kuzniecky Andermann Syndrome
lethal congenital glycogen storage disease of heart
lymphocytic choriomeningitis
Metabolic Brain Diseases +
Mild Encephalitis/Encephalopathy with Reversible Myelin Vacuolization
Myopathy, Epilepsy, and Progressive Cerebral Atrophy
Neonatal Severe Encephalopathy with Lactic Acidosis and Brain Abnormalities
NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND SKELETAL AND BRAIN ABNORMALITIES
NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SLEEP DISTURBANCE, AND BRAIN ABNORMALITIES
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND BRAIN ABNORMALITIES
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, FACIAL DYSMORPHISM, AND BRAIN ABNORMALITIES
NEURODEVELOPMENTAL-CRANIOFACIAL SYNDROME WITH VARIABLE RENAL AND CARDIAC ABNORMALITIES
Non-Lissencephalic Cortical Dysplasia
Postpericardiotomy Syndrome
Progressive Early-Onset Encephalopathy with Episodic Rhabdomyolysis
Progressive Encephalopathy with Amyotrophy and Optic Atrophy
Progressive Encephalopathy, with or without Lipodystrophy
Recurrent Infections, with Encephalopathy, Hepatic Dysfunction, and Cardiovascular Malformations
senile degeneration of brain
Sepsis-Associated Encephalopathy
Thyrocerebral-Retinal Syndrome
transthyretin amyloidosis
Ventricular Dysfunction +
Ventricular Outflow Obstruction +
|
|