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Infantile Neuroaxonal Dystrophy
Infantile neuroaxonal dystrophy
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Neurological disorders
Spinocerebellar ataxia
Neurological disorder
Genetic disorders
Schindler disease
Muscular dystrophy
Genetic disorder
Spinocerebellar ataxia
Disability
Spina bifida
Spinocerebellar ataxia
Muscular dystrophy
Diseases and disorders
(28)
Nakamura osame syndrome
Nanism due to growth hormone combined deficiency
Narrow oral fissure short stature cone shaped epiphyses
Nephronophthisis familial adult spastic quadriparesis
Nephropathy deafness hyperparathyroidism
Nephropathy deafness hyperparathyroidism
Nephropathy familial with hyperuricemia
Nephrosis deafness urinary tract digital malformation
Nephrotic syndrome ocular anomalies
Neuhauser eichner opitz syndrome
Neuraminidase beta-galactosidase deficiency
Neuroaxonal dystrophy renal tubular acidosis
Neuroma biliary tract
Neuronal interstitial dysplasia
Neuropathy motor sensory type 2 deafness mental retardation
Neuropathy sensory spastic paraplegia
Neutropenia intermittent
Neutropenia monocytopenia deafness
Night blindness skeletal anomalies unusual facies
Noble bass sherman syndrome
Non-lissencephalic cortical dysplasia
Noninsulin- -dependent diabetes mellitus with deafness
Nose polyposis familial
Novak syndrome
N-acetyl-g- lucosamine-6-sulfate sulfatase deficiency
Phytanic acid storage disease
Schindler disease
Muscular dystrophy
Spina bifida
more...
See also
PLA2G6
Alpha-N-ac- etylgalactosaminidase
Hallervorden-Spatz disease
Autosomal recessive
NBIA
Pervasive developmental disorder
Phospholipase
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