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Disease Browser
Parent Node:
expandLeukoencephalopathies (D056784)
..Starting node
..expandHereditary Diffuse Leukoencephalopathy with Spheroids (C580150)

       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:5109
Name:Hereditary Diffuse Leukoencephalopathy with Spheroids
Definition:
Alternative IDs:
ParentIDs:MESH:D056784
TreeNumbers:C10.228.140.695/C580150
Synonyms:Adult-Onset Leukodystrophy with Neuroaxonal Spheroids |Autosomal Dominant Leukoencephalopathy with Neuroaxonal Spheroids |Hereditary Diffuse Leukoencephalopathy with Axonal Spheroids |Neuroaxonal Leukodystrophy
Slim Mappings:Nervous system disease
Reference: MedGen: C580150
MeSH: C580150
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants