Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandHypertensive Encephalopathy (D020343)
Parent Node:
expandLeukoencephalopathies (D056784)
..Starting node
..expandPosterior Leukoencephalopathy Syndrome (D054038)

       Child Nodes:



 Sister Nodes: 
..expandAtaxia, Spastic, 3, Autosomal Recessive (C566956)
..expandBrain Small Vessel Disease with Hemorrhage (C564372)
..expandCerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (C563990)
..expandCerebroretinal Microangiopathy with Calcifications and Cysts (C567401)
..expandDementia, Vascular (D015140) Child3
..expandDemyelinating Autoimmune Diseases, CNS (D020278) Child15
..expandGliosis, Familial Progressive Subcortical (C565634)
..expandHereditary Central Nervous System Demyelinating Diseases (D020279) Child29
..expandHereditary Diffuse Leukoencephalopathy with Spheroids (C580150)
..expandLeukodystrophy, Hypomyelinating, with Hypodontia and Hypogonadotropic Hypogonadism (C567313)
..expandLeukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation (C567009)
..expandLEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY (OMIM:613724)
..expandLeukoencephalopathy with Dystonia and Motor Neuropathy, SCPx-Deficient (C566654)
..expandLeukoencephalopathy With Metaphyseal Chondrodysplasia (C567065)
..expandLeukoencephalopathy, Arthritis, Colitis, and Hypogammaglobulinema (C563852)
..expandLeukoencephalopathy, arthritis, colitis, and hypogammaglobulinemia (C535888)
..expandLeukoencephalopathy, Cystic, Without Megalencephaly (C567845)
..expandLeukoencephalopathy, Progressive Multifocal (D007968)
..expandMuscular Dystrophy, Adult-Onset, with Leukoencephalopathy (C565361)
..expandPosterior Leukoencephalopathy Syndrome (D054038)
..expandRibose 5-Phosphate Isomerase Deficiency (C563212)
..expandTelencephalic leukoencephalopathy (C536954)
..expandVanishing White Matter Leukodystrophy with Ovarian Failure (C565836)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:9167
Name:Posterior Leukoencephalopathy Syndrome
Definition:A condition that is characterized by HEADACHE; SEIZURES; and visual loss with edema in the posterior aspects of the CEREBRAL HEMISPHERES, such as the BRAIN STEM. Generally, lesions involve the white matter (nerve fibers) but occasionally the grey matter (nerve cell bodies).
Alternative IDs:
ParentIDs:MESH:D020343|MESH:D056784
TreeNumbers:C10.228.140.631.500.500 |C10.228.140.695.875
Synonyms:Leukoencephalopathy Syndrome, Posterior |Leukoencephalopathy Syndromes, Posterior |Posterior Reversible Encephalopathy Syndrome |Reversible Posterior Leukoencephalopathy Syndrome |Syndrome, Posterior Leukoencephalopathy |Syndromes, Posterior Leukoencephalopat
Slim Mappings:Nervous system disease
Reference: MedGen: D054038
MeSH: D054038
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants