Congenital Disorder

Hereditary Central Nervous System Demyelinating Diseases

AMW:DIS:100081

Inherited conditions characterized by a loss of MYELIN in the central nervous system.

Pathology clinical

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Hereditary Central Nervous System Demyelinating Diseases has parent Brain Diseases, Metabolic, Inborn

Hereditary Central Nervous System Demyelinating Diseases has parent Demyelinating Diseases

Adrenoleukodystrophy has parent Hereditary Central Nervous System Demyelinating Diseases

Alexander Disease has parent Hereditary Central Nervous System Demyelinating Diseases

Canavan Disease has parent Hereditary Central Nervous System Demyelinating Diseases

Leukodystrophy, Globoid Cell has parent Hereditary Central Nervous System Demyelinating Diseases

Leukodystrophy, Metachromatic has parent Hereditary Central Nervous System Demyelinating Diseases

Pelizaeus-Merzbacher Disease has parent Hereditary Central Nervous System Demyelinating Diseases

Hereditary Central Nervous System Demyelinating Diseases has parent Heredodegenerative Disorders, Nervous System

Hereditary Central Nervous System Demyelinating Diseases has parent Leukoencephalopathies

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