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Oculocerebrorenal Syndrome
Oculocerebrorenal syndrome
Overview
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Related in the Kosmos
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Inborn error of metabolism
Ornithine transcarbamylase deficiency
Pyruvate dehydrogenase deficiency
Ochronosis
Diseases and disorders
(38)
Lowe oculocerebrorenal syndrome
Fetofetal transfusion
Glossopharyngeal nerve diseases
Hyperostosis, cortical, congenital
Olfaction disorders
Olfaction disorders
Purpura, schoenlein-henoch
Type i complex regional pain syndrome
Myopathies, structural, congenital
Vulvar neoplasms
Enterocolitis, pseudomembranous
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Physiologic nystagmus
Histiocytosis non-langerhans-cell
Lupus erythematosus, cutaneous
Polyendocr- inopathies, autoimmune
Postpoliomyelitis syndrome
Encephalitis, arbovirus
Intervertebral disk displacement
Rosenthal syndrome
Galactosemias
Optic neuropathy, ischemic
Brachial plexus neuropathies
Ocular motility disorders
Aminoaciduria
Ollier disease
Phosphaturia
Opitz syndrome
Olivoponto- cerebellar atrophy
Cystinosis
Ophthalmoplegia
Tyrosinemia
Mental retardation
Oligohydramnios
Osteomalacia
Obsessive compulsive disorder
Osteogenesis imperfecta
Ochronosis
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Genetic disorders
(10)
Adrenoleuk- odystrophy
Genetic defect
Hyperostosis, cortical, congenital
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Leukodystrophy, globoid cell
Galactosemias
Ochronosis
Cystinosis
Tyrosinemia
Osteogenesis imperfecta
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See also
(20)
Fanconi syndrome
X linked
Solute carrier family
Phosphatid- ylinositol (4,5)-bisphosphate
Phosphatase
Phosphatase
Renal tubular
Dysplasia
Occiput
Birth defects
Syndrome
Cystinuria
Danon disease
Fabry disease
Glucose-6-phosphate dehydrogenase deficiency
Hartnup disease
Hunter syndrome
Iminoglycinuria
Inborn errors of amino acid metabolism
Inborn errors of purine-pyrimidine metabolism
Lesch–Nyhan syndrome
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