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Pelizaeus-- Merzbacher Disease
Pelizaeus-- Merzbacher Disease
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Related in the Kosmos
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Leukodystrophies
Adrenoleuk- odystrophy
Alexander disease
Canavan disease
Krabbe disease
Metachromatic leukodystrophy
Pelizaeus-- merzbacher disease
Zellweger syndrome
Genetic disorders
(40)
Glycogen storage disease type iib
MASA syndrome
Lipid storage disorder
X-linked sideroblastic anemia
Becker's muscular dystrophy
Becker's muscular dystrophy
McLeod syndrome
Aicardi syndrome
Cerebro-oc- ulo-facio-skeletal syndrome
Simpson-Go- labi-Behmel syndrome
Pyruvate dehydrogenase deficiency
Alport syndrome
SCAD deficiency
Propionic acidemia
Androgen insensitivity syndrome
Multiple sulfatase deficiency
Barth syndrome
Parry-Romberg syndrome
Pachyonychia congenita
Pendred syndrome
Progeria
Prader Willi syndrome
Duchenne muscular dystrophy
Adenosine deaminase deficiency
Spinocerebellar ataxia
Pseudoxanthoma elasticum
Peutz-jeghers syndrome
22q11.2 deletion syndrome
Partial trisomy
Stickler syndrome
Spinal muscular atrophy
Charcot-Marie Tooth Disease
Kallmann syndrome
Inherited diseases
Pelizaeus-- merzbacher disease
Adrenoleuk- odystrophy
Leukodystrophies
Alexander disease
Canavan disease
Metachromatic leukodystrophy
Krabbe disease
more...
Diseases and disorders
(56)
Progressive sclerosing poliodystrophy
Polyglucosan body disease adult
Neurological disorders
Progressive osseous heteroplasia
Leukodystrophy
Leukodystrophy
Focal dermal hypoplasia
Demyelination
X-linked lymphoproliferative disease
Dysmyelination
Infantile Refsum disease
Spongioblastoma
X-linked hypophosphatemia
Hypomyelination
Physiologic nystagmus
X-linked ichthyosis
Sotos syndrome
Dysostosis
CHILD syndrome
Pneumonic plague
Parkinson disease
Dystonia
Progressive supranuclear palsy
Rare diseases
Acute disseminated encephalomyelitis
Phantom limb
Paget's disease of bone
Multiple system atrophy
Pelizaeus-- merzbacher disease
Glycogen storage disease type iib
MASA syndrome
Lipid storage disorder
X-linked sideroblastic anemia
Becker's muscular dystrophy
Cerebro-oc- ulo-facio-skeletal syndrome
Pyruvate dehydrogenase deficiency
Alport syndrome
Alexander disease
Canavan disease
Androgen insensitivity syndrome
Multiple sulfatase deficiency
Barth syndrome
Parry-Romberg syndrome
Pendred syndrome
Progeria
Prader Willi syndrome
Metachromatic leukodystrophy
Duchenne muscular dystrophy
Adenosine deaminase deficiency
Pseudoxanthoma elasticum
Krabbe disease
22q11.2 deletion syndrome
Partial trisomy
Stickler syndrome
Spinal muscular atrophy
Charcot-Marie Tooth Disease
Kallmann syndrome
more...
Lysosomal storage diseases
(40)
Alpha-mannosidosis
Aspartylgl- ucosaminuria
Batten disease
Canavan disease
Cholesteryl ester storage disease
Cholesteryl ester storage disease
Cystinosis
Fabry disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Galactosialidosis
Gangliosidosis
Gaucher's disease
Glycogen storage disease type iib
Glycoproteinosis
Hunter syndrome
Hurler syndrome
I-cell disease
Krabbe disease
Lipid storage disorder
Lysosomal storage disease
Metachromatic leukodystrophy
Morquio syndrome
Mucolipidosis
Mucolipidosis type IV
Mucopolysa- ccharidosis
Multiple sulfatase deficiency
Neuronal ceroid lipofuscinosis
Niemann-Pick disease, type C
Niemann–Pick disease
Pseudo-Hurler polydystrophy
Pycnodysostosis
Salla disease
Sandhoff disease
Sanfilippo syndrome
Schindler disease
Sialidosis
Sly syndrome
Tay-Sachs disease
Wolman disease
more...
Inborn errors of metabolism
(8)
Glycogen storage disease type iib
Lipid storage disorder
Infantile Refsum disease
SCAD deficiency
Propionic acidemia
Propionic acidemia
X-linked ichthyosis
Adenosine deaminase deficiency
Krabbe disease
more...
Autosomal recessive disorders
(12)
Glycogen storage disease type iib
Lipid storage disorder
Cerebro-oc- ulo-facio-skeletal syndrome
SCAD deficiency
Propionic acidemia
Propionic acidemia
Canavan disease
Multiple sulfatase deficiency
Pendred syndrome
Metachromatic leukodystrophy
Adenosine deaminase deficiency
Pseudoxanthoma elasticum
Krabbe disease
more...
Neurology
(12)
Myoclonic Encephalopathy of infants
Acquired epileptiform aphasia
Neural stem cells
Central nervous system
Oligodendrocyte
Oligodendrocyte
Neuropathology
Adrenoleuk- odystrophy
Neurological disorders
Demyelination
Spongioblastoma
Dystonia
Acute disseminated encephalomyelitis
more...
Extrapyramidal and movement disorders
(19)
Hallervorden-Spatz disease
Akathisia
Blepharospasm
Choreia (disease)
Dystonia
Dystonia
Essential tremor
Meige's syndrome
Movement disorder
Multiple system atrophy
Myoclonus
Neuroleptic malignant syndrome
Parkinson disease
Parkinsonism
Postencephalitic parkinsonism
Progressive supranuclear palsy
Restless legs syndrome
Spasmodic torticollis
Stiff person syndrome
Tardive dyskinesia
more...
Genetics
X linked
X-linked recessive
Mutation
Inherited diseases
See also
(20)
Hyper IgM Syndrome Type 1
Ludwig Merzbacher
Myelin
Myelinogenesis
Hirayama syndrome
Hirayama syndrome
Autosomal dominant
Autosomal recessive
Pellucid Marginal Degeneration
The Myelin Project
The Stennis Foundation
X-Linked mental retardation
X-linked alpha thalassemia mental retardation syndrome
X-linked spinal muscular atrophy 2
Pallister
KAL1
Congenital malformations
Pierre Robin (surgeon)
Immune disorders
White matter
Spasticity
more...
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