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neurofibromatosis
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neurofibromatosis
noun
(neu-ro-fi-bro-ma-to-sis)
a disorder inherited as an autosomal dominant and characterized especially by brown spots on the skin, neurofibromas of peripheral nerves, and deformities of subcutaneous tissue and bone
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neurofibromatosis
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genetic disorder
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muscular dystrophy
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degenerative disorder
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neuroblastoma
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leukodystrophy
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neurofibroma
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osteogenesis imperfecta
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juvenile diabetes
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dystrophy
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cystic fibrosis
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retinoblastoma
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rhabdomyosarcoma
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epilepsy
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leukemia
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achondroplasia
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autoimmune disease
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alopecia areata
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cerebral palsy
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syringomyelia
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carcinoid
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spina bifida
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sarcoma
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dwarfism
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scleroderma
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lymphoma
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progeria
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medulloblastoma
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metabolic disorder
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amyotrophic lateral sclerosis
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osteopetrosis
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tumor
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malformation
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hemangioma
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ataxia
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astrocytoma
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meningioma
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amyloidosis
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dysplasia
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lupus
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polycystic kidney disease
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histiocytosis
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embryonal rhabdomyosarcoma
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blastoma
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alopecia
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congenital disorder
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lymphoblastic leukemia
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osteogenic sarcoma
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lymphocytic leukemia
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alveolar rhabdomyosarcoma
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neurological disorder
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leiomyosarcoma
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retinitis pigmentosa
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brain tumor
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myotonic dystrophy
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juvenile rheumatoid arthritis
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ichthyosis
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myotonic muscular dystrophy
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angiosarcoma
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scoliosis
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aplastic anemia
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acute lymphoblastic leukemia
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wilms tumour
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autosomal dominant disease
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cancer
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becker muscular dystrophy
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aplastic anaemia
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autosomal dominant disorder
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vasculitis
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diaphragmatic hernia
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myasthenia gravis
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myositis
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hydrocephalus
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autism
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acute lymphocytic leukemia
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acute myeloid leukemia
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fibroma
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genetic abnormality
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duchenne
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cerebri
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hypertrichosis
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achromatopsia
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nephritis
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severe combined immunodeficiency
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glomerulonephritis
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retinitis
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polymyositis
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teratoma
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apraxia
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choriocarcinoma
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neuropathies
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hemolytic anemia
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rheumatic disease
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dermoid cyst
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multiple sclerosis
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prosopagnosia
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autoimmune disorder
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microcephaly
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immunodeficiency
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chromosomal anomaly
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acromegaly
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neurofibromatosis
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