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Phytanic Acid Storage Disease
Phytanic acid storage disease
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Genodermatoses
Distal Arthrogryposis, Type IIA
4p- syndrome
Rhizomelic chondrodysplasia punctata
Dyskeratosis congenita
Ichthyosis
Progeria
Inborn errors of metabolism
Leukodystrophy, globoid cell
Galactosemias
Diseases and disorders
(44)
Progressive sclerosing poliodystrophy
Polyglucosan body disease adult
Neurological disorders
Glossopharyngeal nerve diseases
Hyperostosis, cortical, congenital
Hyperostosis, cortical, congenital
Purpura, schoenlein-henoch
Type i complex regional pain syndrome
Myopathies, structural, congenital
Hemifacial atrophy progressive
Enterocolitis, pseudomembranous
Hereditary sensory and autonomic neuropathies
Physiologic nystagmus
Fetofetal transfusion
Histiocytosis non-langerhans-cell
Lupus erythematosus, cutaneous
Polyendocr- inopathies, autoimmune
Postpoliomyelitis syndrome
Encephalitis, arbovirus
Olfaction disorders
Intervertebral disk displacement
Intracranial cyst
Rosenthal syndrome
Brachial plexus neuropathies
Peroxisomal disorder
Diencephalic syndrome
Optic neuropathy, ischemic
5p- syndrome
Retinitis pigmentosa
Progressive supranuclear palsy
Porphyria cutanea tarda
Partial trisomy
Dystonia
Temporal arteritis
Encephalomyelitis
Friedreich's ataxia
Motor neurone disease
Dwarfism
Leukodystrophy, globoid cell
Distal Arthrogryposis, Type IIA
Galactosemias
Rhizomelic chondrodysplasia punctata
Dyskeratosis congenita
Ichthyosis
Progeria
more...
Genetic disorders
(16)
Adrenoleuk- odystrophy
Leukodystrophies
Monosomy
Genetic disorder
Hyperostosis, cortical, congenital
Hyperostosis, cortical, congenital
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Galactosemias
4p- syndrome
5p- syndrome
Dyskeratosis congenita
Retinitis pigmentosa
Porphyria cutanea tarda
Partial trisomy
Friedreich's ataxia
Progeria
more...
Neurology
(8)
Myoclonic Encephalopathy of infants
Ramsay Hunt syndrome type I
Acquired epileptiform aphasia
Neurodegenerative disorder
Adrenoleuk- odystrophy
Adrenoleuk- odystrophy
Neurological disorders
Dystonia
Temporal arteritis
more...
Neurological disorders
(9)
Progressive sclerosing poliodystrophy
Hereditary sensory and autonomic neuropathies
Olfaction disorders
Intracranial cyst
Leukodystrophies
Leukodystrophies
Encephalomyelitis
Neurodegenerative disorder
Friedreich's ataxia
Motor neurone disease
more...
Motor neuron disease
(11)
Hirayama syndrome
ALS Association
ALS Society of Canada
Amyotrophic lateral sclerosis
Motor neurone disease
Motor neurone disease
People with motor neuron disease
Postpoliomyelitis syndrome
Primary lateral sclerosis
Spinal muscular atrophy
Split hand syndrome
Survival motor neuron spinal muscular atrophy
more...
See also
(17)
Phytanic acid
Biology
Phytanoyl-CoA hydroxylase
PEX1
PEX7
PEX7
Chemical substances
Pristanic acid
Cornification
Dentin dysplasia
Pierre Robin (surgeon)
Objects
The Myelin Project
IRD asset
Pallister
9P
6Q
Hypertrophy
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