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Pelizaeus-- Merzbacher Disease
Pelizaeus-- Merzbacher Disease
Overview
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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
(35)
Glycogen storage disease type iib
MASA syndrome
X-linked sideroblastic anemia
Becker's muscular dystrophy
Lipid storage disorder
Lipid storage disorder
Aicardi syndrome
Simpson-Go- labi-Behmel syndrome
Cerebro-oc- ulo-facio-skeletal syndrome
McLeod syndrome
Pyruvate dehydrogenase deficiency
Alport syndrome
Mendelian disorder
Lelis syndrome
Barth syndrome
Androgen insensitivity syndrome
Trinucleotide repeat disorders
Multiple sulfatase deficiency
Parry-Romberg syndrome
Pachyonychia congenita
Pendred syndrome
Adenosine deaminase deficiency
Haemophilia
X-linked dominant
22q11.2 deletion syndrome
Adrenomyel- oneuropathy
Charcot-Marie Tooth Disease
Wiskott-aldrich syndrome
Batten disease
Pelizaeus-- merzbacher disease
Adrenoleuk- odystrophy
Leukodystrophies
Alexander disease
Canavan disease
Metachromatic leukodystrophy
Krabbe disease
more...
Diseases and disorders
(47)
Progressive sclerosing poliodystrophy
Neurological disorders
Leukodystrophy
Phytanic acid storage disease
Focal dermal hypoplasia
Focal dermal hypoplasia
X-linked lymphoproliferative disease
X-linked hypophosphatemia
Demyelination
X-linked ichthyosis
Centronuclear myopathy
Hypomyelination
Physiologic nystagmus
Hypohidrotic ectodermal dysplasia
CHILD syndrome
Incontinentia pigmenti
Ataxia
Progressive supranuclear palsy
Dystonia
Acute disseminated encephalomyelitis
Temporal arteritis
Rare diseases
Phantom limb
Paget's disease of bone
Pelizaeus-- merzbacher disease
Glycogen storage disease type iib
MASA syndrome
X-linked sideroblastic anemia
Becker's muscular dystrophy
Lipid storage disorder
Cerebro-oc- ulo-facio-skeletal syndrome
Pyruvate dehydrogenase deficiency
Alport syndrome
Alexander disease
Barth syndrome
Androgen insensitivity syndrome
Multiple sulfatase deficiency
Canavan disease
Parry-Romberg syndrome
Pendred syndrome
Adenosine deaminase deficiency
Metachromatic leukodystrophy
Haemophilia
Krabbe disease
22q11.2 deletion syndrome
Charcot-Marie Tooth Disease
Wiskott-aldrich syndrome
Batten disease
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
Glycogen storage disease type iib
Lipid storage disorder
Phytanic acid storage disease
X-linked ichthyosis
Adenosine deaminase deficiency
Krabbe disease
Autosomal recessive disorders
(10)
Glycogen storage disease type iib
Lipid storage disorder
Cerebro-oc- ulo-facio-skeletal syndrome
Multiple sulfatase deficiency
Canavan disease
Canavan disease
Pendred syndrome
Adenosine deaminase deficiency
Metachromatic leukodystrophy
Krabbe disease
Batten disease
more...
Neurology
(12)
Myoclonic Encephalopathy of infants
Ramsay Hunt syndrome type I
Acquired epileptiform aphasia
Central nervous system
Oligodendrocyte
Oligodendrocyte
Adrenoleuk- odystrophy
Neurological disorders
Demyelination
Neurodegenerative
Dystonia
Acute disseminated encephalomyelitis
Temporal arteritis
more...
Genetics
X linked
X-linked recessive
Mutation
Mendelian disorder
See also
(20)
Hyper IgM Syndrome Type 1
Ludwig Merzbacher
Hirayama syndrome
Myelin
Pellucid Marginal Degeneration
Pellucid Marginal Degeneration
Autosomal dominant
Autosomal recessive
The Stennis Foundation
KAL1
The Myelin Project
X-Linked mental retardation
X-linked alpha thalassemia mental retardation syndrome
X-linked spinal muscular atrophy 2
Gfp-cdna
Congenital malformations
Mitocheck
Immune disorders
Online Mendelian Inheritance in Animals
Hallervorden-Spatz disease
Mendelian Inheritance in Man
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