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| Similar words: Sjogren's Syndrome | |
| Hallermann's Syndrome Hallermann-Streiff Syndrome | Hallermann Streiff Syndrome | Hallermann Syndrome | Hallermanns Syndrome | Syndrome, Hallermann' | s | Syndrome, Hallermann-Streiff An oculomandibulofacial syndrome principally characterized by dyscephaly (usually brachycephaly), parrot nose, mandibular hypoplasia, proportionate nanism, hypotrichosis, bilateral congenital cataracts, and microphthalmia. (Dorland, 27th ed) | |
| Wissler's Syndrome Subsepsis Allergica | Subsepsis Hyperergica | Wissler-Fanconi Syndrome | Syndrome, Wissler' | s | Syndrome, Wissler-Fanconi | Wissler Fanconi Syndrome | Wissler Syndrome | Wisslers Syndrome A rheumatic syndrome of possibly allergic origin, usually affecting children and adolescents, and characterized by high fever, exanthema, arthralgia, leukocytosis, and increased sedimentation rate. | |
| Antibodies, Antinuclear Anti-DNA Antibodies | Antibodies, Anti-DNA | Antinuclear Antibodies | Antinuclear Factors | Fluorescent Antinuclear Antibodies | Antinuclear Antibody | Antinuclear Factor | Anti DNA Antibodies | Antibodies, Anti DNA | Antibody, Antinuclear Autoantibodies directed against various nuclear antigens including DNA, RNA, histones, acidic nuclear proteins, or complexes of these molecular elements. Antinuclear antibodies are found in systemic autoimmune diseases including systemic lupus erythematosus, Sjogren's syndrome, scleroderma, polymyositis, and mixed connective tissue disease. | |
| Sweating, Gustatory Auriculotemporal Syndrome | Baillarger Syndrome | Frey Syndrome | Hyperhidrosis, Gustatory | Frey' | s Syndrome | Salivosudoriparous Syndrome | Von Frey Syndrome | Von Frey' | s Syndrome | Freys Syndrome | Gustatory Hyperhidroses An autonomic disorder characterized by excessive sweating of the forehead, upper lip, perioral region, or sternum subsequent to gustatory stimuli. The auriculotemporal syndrome features facial flushing or sweating limited to the distribution of the auriculotemporal nerve and may develop after trauma to the parotid gland, in association with PAROTID NEOPLASMS, or following their surgical removal. (From Ann Neurol 1997 Dec;42(6):973-5) | |
| Euthyroid Sick Syndromes High T4 Syndrome | Low T3 Syndrome | Low T3 and T4 Syndrome | Low T3 High T4 Syndrome | Low T3-High T4 Syndrome | Euthyroid Sick Syndrome | High T4 Syndromes | Low T3 Syndromes | Syndrome, Euthyroid Sick | Syndrome, High T4 | Syndrome, Low T3 Abnormalities in thyroid hormone and thyroid-stimulating hormone levels, often simulating hypothyroidism, in euthyroid patients suffering some other illness, such as diabetes mellitus or liver cirrhosis. | |
| Acrocephalosyndactylia Apert Syndrome | Pfeiffer Syndrome | Saethre-Chotzen Syndrome | Acrocephalosyndactylias | Saethre Chotzen Syndrome | Syndrome, Apert | Syndrome, Pfeiffer | Syndrome, Saethre-Chotzen Craniostenosis characterized by acrocephaly and syndactyly, probably occurring as an autosomal dominant trait and usually as a new mutation. (Dorland, 27th ed) | |
| Cockayne Syndrome Progeria-Like Syndrome | Cockayne Syndrome, Group A | Cockayne Syndrome, Group B | Cockayne Syndrome, Group C | Cockayne Syndrome, Type A | Cockayne Syndrome, Type B | Cockayne Syndrome, Type C | Cockayne Syndrome, Type I | Syndrome, Cockayne An inherited syndrome phenotypically characterized by unusual facies (large ears and sunken eyes), growth failure, intellectual deterioration, loss of subcutaneous fat, pigmentary retinal degeneration, neural deafness, dwarfism, photosensitivity, optic atrophy, peripheral neuropathy, and cataracts. Pathologic examination reveals a patchy loss of central myelin and white matter atrophy. Cockayne syndrome may be divided into two or more distinct genetic subtypes. (Menkes, Textbook of Child Neurology, 5th ed, p197) | |
| Laurence-Moon Syndrome Laurence-Moon-Biedl Syndrome | Laurence Moon Biedl Syndrome | Laurence Moon Syndrome | Syndrome, Laurence-Moon | Syndrome, Laurence-Moon-Biedl An autosomal recessive condition characterized by hypogonadism; spinocerebellar degeneration; MENTAL RETARDATION; RETINITIS PIGMENTOSA; and OBESITY. This syndrome was previously referred to as Laurence-Moon-Biedl syndrome until BARDET-BIEDL SYNDROME was identified as a distinct entity. (From N Engl J Med. 1989 Oct 12;321(15):1002-9) | |
| Munchausen Syndrome Hospital-Addiction Syndrome | Munchhausen Syndrome | Syndrome, Hospital-Addiction | Hospital Addiction Syndrome | Hospital-Addiction Syndromes | Syndrome, Hospital Addiction | Syndrome, Munchausen | Syndrome, Munchhausen A factitious disorder characterized by habitual presentation for hospital treatment of an apparent acute illness, the patient giving a plausible and dramatic history, all of which is false. | |
| Orofaciodigital Syndromes Gorlin-Psaume Syndrome | Mohr Syndrome | Papillon-Leage and Psaume Syndrome | Gorlin Psaume Syndrome | Orofaciodigital Syndrome | Papillon Leage and Psaume Syndrome | Syndrome, Gorlin-Psaume | Syndrome, Mohr | Syndrome, Orofaciodigital Two syndromes of oral, facial, and digital malformations. Type I (Papillon-Leage and Psaume syndrome, Gorlin-Psaume syndrome) is inherited as an X-linked dominant trait and is found only in females and XXY males. Type II (Mohr syndrome) is inherited as an autosomal recessive trait. | |
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