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Lesch-nyhan Syndrome
Lesch-nyhan syndrome
Overview
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Related in the Kosmos
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Inborn errors of metabolism
(8)
Glycogen storage disease type iib
Lipid storage disorder
Long-chain 3-hydroxya- cyl-coenzyme A dehydrogenase deficiency
Glutaricaciduria
Sly syndrome
Sly syndrome
Leukodystrophy, globoid cell
Phenylketonuria
Galactosemias
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Skin conditions resulting from errors in metabolism
Adrenoleuk- odystrophy
Phenylketonuria
Pediatrics
Lamellar ichthyosis
Hyperostosis, cortical, congenital
Purpura, schoenlein-henoch
Denver Developmental Screening Test
Rare diseases
Legg-perthes disease
Lambert eaton syndrome
Lamellar ichthyosis
Glycogen storage disease type iib
Lipid storage disorder
Sly syndrome
Leukodystrophy, globoid cell
Syndromes
(8)
Leopard syndrome
Androgen insensitivity syndrome
Lentiginosis
Hereditary sensory and autonomic neuropathies
Fetofetal transfusion
Fetofetal transfusion
McLeod syndrome
Alport syndrome
Sly syndrome
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Genetic disorders
(28)
X-linked sideroblastic anemia
MASA syndrome
Langer-giedion syndrome
Simpson-Go- labi-Behmel syndrome
Becker's muscular dystrophy
Becker's muscular dystrophy
Aicardi syndrome
Pyruvate dehydrogenase deficiency
Laurence Moon syndrome
Adenine phosphorib- osyltransferase deficiency
Loken Senior syndrome
Thrombocytopenia absent radius
Leopard syndrome
Adrenoleuk- odystrophy
Lamellar ichthyosis
Glycogen storage disease type iib
Androgen insensitivity syndrome
Lipid storage disorder
Long-chain 3-hydroxya- cyl-coenzyme A dehydrogenase deficiency
Glutaricaciduria
Hyperostosis, cortical, congenital
Lentiginosis
Sly syndrome
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
McLeod syndrome
Phenylketonuria
Galactosemias
Alport syndrome
more...
Medical condition
(60)
Leiomyoma
Lipoid nephrosis
Lateral epicondylitis
Leukemic reticuloen- dotheliosis
Late syphilis
Late syphilis
Lesch-nyhan disease
Hyperuricemia
Acute biphenotypic leukemia
Reticular dysgenesis
Progressive sclerosing poliodystrophy
Lymphohistiocytosis
Myelofibrosis
Craniofrontonasal dysplasia
Glossopharyngeal nerve diseases
Floating harbor syndrome
Type i complex regional pain syndrome
Myopathies, structural, congenital
Enterocolitis, pseudomembranous
Physiologic nystagmus
Histiocytosis non-langerhans-cell
Lancereaux- -Mathieu-Weil Spirochetosis
Lupus erythematosus, cutaneous
Polyendocr- inopathies, autoimmune
Postpoliomyelitis syndrome
Hypoxanthine guanine phosphorib- osyltransferase deficiency
Encephalitis, arbovirus
Olfaction disorders
Intervertebral disk displacement
Alzheimer disease type 2
Rosenthal syndrome
Amyotrophic lateral sclerosis type 2
Lenz microphthalmia syndrome
Uric acid nephrolithiasis
Focal dermal hypoplasia
Phytanic acid storage disease
Leukemia
Lowe syndrome
X-linked lymphoproliferative disease
Legg-perthes disease
Lambert eaton syndrome
Lamellar ichthyosis
Glycogen storage disease type iib
X-linked sideroblastic anemia
Androgen insensitivity syndrome
Glutaricaciduria
Hyperostosis, cortical, congenital
Purpura, schoenlein-henoch
Langer-giedion syndrome
Lentiginosis
Becker's muscular dystrophy
Sly syndrome
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Fetofetal transfusion
Pyruvate dehydrogenase deficiency
Phenylketonuria
Adenine phosphorib- osyltransferase deficiency
Galactosemias
Alport syndrome
Thrombocytopenia absent radius
more...
Lysosomal storage diseases
(40)
Mucolipidosis II
Alpha-mannosidosis
Aspartylgl- ucosaminuria
Batten disease
Canavan disease
Canavan 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
Leukodystrophy, globoid cell
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
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Diseases and disorders
(10)
Letterer-Siwe disease
X-linked hypophosphatemia
Juvenile primary lateral sclerosis
X-linked sideroblastic anemia
MASA syndrome
MASA syndrome
Lymphohistiocytosis
Lipid storage disorder
Leukodystrophy, globoid cell
Lupus erythematosus, cutaneous
Pyruvate dehydrogenase deficiency
more...
See also
(20)
Diseases and disorders
Limited range of motion
Lack of strength
Lateral collateral ligament
Ovovegetarian
Ovovegetarian
Leukemoid reaction
Lactovegetarian
Hyper IgM Syndrome Type 1
Langerhans cell
Livedo reticularis
X-linked recessive
Kelley-Seegmiller syndrome
Hypoxanthi- ne-guanine phosphorib- osyltransferase
Mycophenolate
X linked
Urate
Tophi
Purines
Purine
Hirayama syndrome
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