Kosmix
One sec... we're building your guide for
Infantile Refsum Disease
Infantile Refsum disease
Overview
Tools
Health Providers & Organizations
Main ›
Tools
›
Skinsight
Body Location Disease Search
Related in the Kosmos
?
Inborn errors of metabolism
Leukodystrophy, globoid cell
Zellweger syndrome
Galactosemias
Diseases and disorders
(40)
Refsum disease infantile form
Progressive sclerosing poliodystrophy
Hyperpipecolic acidemia
Neurological disorders
Peroxisome biogenesis disorders
Peroxisome biogenesis disorders
Glossopharyngeal nerve diseases
Hyperostosis, cortical, congenital
Purpura, schoenlein-henoch
Type i complex regional pain syndrome
Myopathies, structural, congenital
Enterocolitis, pseudomembranous
Hereditary sensory and autonomic neuropathies
Fetofetal transfusion
Histiocytosis non-langerhans-cell
Rosenthal syndrome
Lupus erythematosus, cutaneous
Physiologic nystagmus
Polyendocr- inopathies, autoimmune
Postpoliomyelitis syndrome
Encephalitis, arbovirus
Olfaction disorders
Hemifacial atrophy progressive
Rhizomelic chondrodysplasia punctata
Intervertebral disk displacement
Pseudo-zellweger syndrome
Intracranial cyst
Brachial plexus neuropathies
Optic neuropathy, ischemic
Alexander disease
Retinitis pigmentosa
Bardet Biedl Syndrome
Agammaglobulinemia
Canavan disease
Temporal arteritis
Ataxia
Encephalomyelitis
Rhabdomyosarcoma
Leukodystrophy, globoid cell
Zellweger syndrome
Galactosemias
more...
Leukodystrophies
Neonatal adrenoleuk- odystrophy
Alexander disease
Canavan disease
Leukodystrophy, globoid cell
Metachromatic leukodystrophy
Pelizaeus-- Merzbacher disease
Zellweger syndrome
Genetic disorders
(13)
Genetic disorder
Neonatal adrenoleuk- odystrophy
Hyperpipecolic acidemia
Hyperostosis, cortical, congenital
Leukodystrophy, globoid cell
Leukodystrophy, globoid cell
Zellweger syndrome
Hereditary sensory and autonomic neuropathies
Galactosemias
Leukodystrophies
Alexander disease
Retinitis pigmentosa
Bardet Biedl Syndrome
Canavan disease
more...
Neurology
Ramsay Hunt syndrome type I
Myoclonic Encephalopathy of infants
Ramsay Hunt syndrome type II
Neonatal adrenoleuk- odystrophy
Neurological disorders
Temporal arteritis
Neurological disorders
Progressive sclerosing poliodystrophy
Hereditary sensory and autonomic neuropathies
Olfaction disorders
Intracranial cyst
Leukodystrophies
Ataxia
Encephalomyelitis
Gene
PEX1
PEX2
PEX12
PEX5
PEX19
PEX14
PEX13
See also
(14)
Phytanic acid
Hirayama syndrome
Vasospasm, intracranial
PEX26
Phytanoyl-CoA hydroxylase
Phytanoyl-CoA hydroxylase
PEX7
Biogenesis
Peroxisomal
Peroxin
The Myelin Project
PBDS
IBM mainframe
NINDS
Phenotype
more...
more categories...
Health Providers & Organizations
›
Vitals.com
