DeCS 2000 - Changed terms
|
Replaced |
Replaced-by |
| ACOUSTIC NERVE | VESTIBULOCOCHLEAR NERVE |
| ACOUSTIC NERVE DISEASES | VESTIBULOCOCHLEAR NERVE DISEASES |
| ADIE'S SYNDROME | ADIE SYNDROME |
| AMYGDALOID BODY | AMYGDALA |
| ANDROGEN-BINDING PROTEINS | ANDROGEN-BINDING PROTEIN |
| ANOSMIA | OLFACTION DISORDERS |
| APRAXIA | APRAXIAS |
| ARNOLD-CHIARI DEFORMITY | ARNOLD-CHIARI MALFORMATION |
| ASPARTIC PROTEINASES | ASPARTIC ENDOPEPTIDASES |
| CALLUS | BONY CALLUS |
| CEREBELLAR DYSSYNERGIA | MYOCLONIC CEREBELLAR DYSSYNERGIA |
| CEREBRAL ANEURYSM | INTRACRANIAL ANEURYSM |
| CEREBRAL ANOXIA | HYPOXIA, BRAIN |
| CEREBRAL ARTERIOSCLEROSIS | INTRACRANIAL ARTERIOSCLEROSIS |
| CEREBRAL ARTERIOVENOUS MALFORMATIONS | INTRACRANIAL ARTERIOVENOUS MALFORMATIONS |
| CEREBRAL ARTERY DISEASES | CEREBRAL ARTERIAL DISEASES |
| CEREBRAL EMBOLISM AND THROMBOSIS | INTRACRANIAL EMBOLISM AND THROMBOSIS |
| CEREBRAL ISCHEMIA | BRAIN ISCHEMIA |
| CEREBRAL ISCHEMIA, TRANSIENT | ISCHEMIC ATTACK, TRANSIENT |
| CEREBRAL SCLEROSIS, DIFFUSE | DIFFUSE CEREBRAL SCLEROSIS OF SCHILDER |
| CEREBROSPINAL OTORRHEA | CEREBROSPINAL FLUID OTORRHEA |
| CEREBROSPINAL RHINORRHEA | CEREBROSPINAL FLUID RHINORRHEA |
| CHARCOT-MARIE DISEASE | CHARCOT-MARIE-TOOTH DISEASE |
| CHORDATA | CHORDATA, NONVERTEBRATE |
| COGNITIVE SYMPTOMS | NEUROBEHAVIORAL MANIFESTATIONS |
| CONVULSIONS, FEBRILE | SEIZURES, FEBRILE |
| CYSTEINE PROTEINASES | CYSTEINE ENDOPEPTIDASES |
| DATAPHONE | MODEMS |
| DE LANGE'S SYNDROME | DE LANGE SYNDROME |
| DEITERS NUCLEUS | VESTIBULAR NUCLEUS, LATERAL |
| DOUBLE BIND THEORY | DOUBLE BIND INTERACTION |
| DUANE'S SYNDROME | DUANE RETRACTION SYNDROME |
| ENCEPHALITIS, EPIDEMIC | ENCEPHALITIS, ARBOVIRUS |
| ENCEPHALOMYELITIS, ALLERGIC | ENCEPHALOMYELITIS, EXPERIMENTAL AUTOIMMUNE |
| EPIDERMAL GROWTH FACTOR-UROGASTRONE | EPIDERMAL GROWTH FACTOR |
| EPILEPSY, MYOCLONIC | EPILEPSIES, MYOCLONIC |
| EPILEPSY, PARTIAL | EPILEPSIES, PARTIAL |
| ESTHESIONEUROBLASTOMA | ESTHESIONEUROBLASTOMA, OLFACTORY |
| FICIN | FICAIN |
| FOURNIER'S GANGRENE | FOURNIER GANGRENE |
| FRIEDREICH'S ATAXIA | FRIEDREICH ATAXIA |
| FUCOSIDASE | ALPHA-L-FUCOSIDASE |
| GALACTOSEMIA | GALACTOSEMIAS |
| GANGLIOSIDOSIS G(M1) | GANGLIOSIDOSIS GM1 |
| GAUCHER'S DISEASE | GAUCHER DISEASE |
| GENES, WILMS' TUMOR | GENES, WILMS TUMOR |
| GERSTMANN'S SYNDROME | GERSTMANN SYNDROME |
| GERSTMANN-STRAUSSLER SYNDROME | GERSTMANN-STRAUSSLER-SCHEINKER DISEASE |
| GILBERT'S DISEASE | GILBERT DISEASE |
| HEAD INJURIES | CRANIOCEREBRAL TRAUMA |
| HEART HYPERTROPHY | CARDIOMEGALY |
| HIGH PRESSURE NERVOUS SYNDROME | HIGH PRESSURE NEUROLOGICAL SYNDROME |
| HORNER'S SYNDROME | HORNER SYNDROME |
| HUNTINGTON'S DISEASE | HUNTINGTON DISEASE |
| HYPERSOMNIA | DISORDERS OF EXCESSIVE SOMNOLENCE |
| HYPOTHALAMIC AREA, ANTERIOR | ANTERIOR HYPOTHALAMIC NUCLEUS |
| IDITOL DEHYDROGENASE | L-IDITOL 2-DEHYDROGENASE |
| INJURIES, POISONINGS, AND OCCUPATIONAL DISEASES | DISORDERS OF ENVIRONMENTAL ORIGIN |
| INSOMNIA | SLEEP INITIATION AND MAINTENANCE DISORDERS |
| INTERFERON ALFA, RECOMBINANT | INTERFERON TYPE I, RECOMBINANT |
| KALLIKREIN | KALLIKREINS |
| KINKY HAIR SYNDROME | MENKES KINKY HAIR SYNDROME |
| LAURENCE-MOON-BIEDL SYNDROME | LAURENCE-MOON SYNDROME |
| MAXIMUM PERMISSIBLE EXPOSURE LEVEL | MAXIMUM ALLOWABLE CONCENTRATION |
| MENSTRUATION DISORDERS | MENSTRUATION DISTURBANCES |
| METALLOPROTEINASES | METALLOENDOPEPTIDASES |
| MITOMYCIN C | MITOMYCIN |
| MUCOLIPIDOSIS | MUCOLIPIDOSES |
| MUSCULAR DYSTROPHY | MUSCULAR DYSTROPHIES |
| MYOTONIA ATROPHICA | MYOTONIC DYSTROPHY |
| NEMALINE MYOPATHY | MYOPATHIES, NEMALINE |
| NERVOUS SYSTEM ABNORMALITIES | NERVOUS SYSTEM MALFORMATIONS |
| NEUROECTODERMAL TUMOR, PERIPHERAL | NEUROECTODERMAL TUMORS, PRIMITIVE, PERIPHERAL |
| NEUROECTODERMAL TUMOR, PRIMITIVE | NEUROECTODERMAL TUMORS, PRIMITIVE |
| NEUROFIBROMATOSIS | NEUROFIBROMATOSES |
| NEUROPATHIES, HEREDITARY MOTOR AND SENSORY | HEREDITARY MOTOR AND SENSORY NEUROPATHIES |
| NEUROPATHIES, HEREDITARY SENSORY AND AUTONOMIC | HEREDITARY SENSORY AND AUTONOMIC NEUROPATHIES |
| NIEMANN-PICK DISEASE | NIEMANN-PICK DISEASES |
| NYSTAGMUS | NYSTAGMUS, PATHOLOGIC |
| OCULOMOTOR NERVE PARALYSIS | OCULOMOTOR NERVE DISEASES |
| OLIVOPONTOCEREBELLAR ATROPHY | OLIVOPONTOCEREBELLAR ATROPHIES |
| OPTIC ATROPHY, HEREDITARY | OPTIC ATROPHIES, HEREDITARY |
| OXYTOCINASE | CYSTINYL AMINOPEPTIDASE |
| P42(MAPK) KINASE | P42 MAP KINASE |
| PANCREATOPEPTIDASE | PANCREATIC ELASTASE |
| PARALYSIS, BULBAR | BULBAR PALSY, PROGRESSIVE |
| PARALYSIS, FAMILIAL PERIODIC | PARALYSES, FAMILIAL PERIODIC |
| PARKINSON DISEASE, SYMPTOMATIC | PARKINSON DISEASE, SECONDARY |
| PEPTIDE PEPTIDOHYDROLASES | ENDOPEPTIDASES |
| PERIODIC DISEASE | FAMILIAL MEDITERRANEAN FEVER |
| PERIPHERAL NERVE NEOPLASMS | PERIPHERAL NERVOUS SYSTEM NEOPLASMS |
| PHENYLKETONURIA | PHENYLKETONURIAS |
| POLYNEURITIS | POLYNEUROPATHIES |
| POLYRADICULITIS | POLYRADICULOPATHY |
| POLYRADICULONEURITIS | POLYRADICULONEUROPATHY |
| PROTO-ONCOGENE PROTEINS C-ERBB-2 | RECEPTOR, ERBB-2 |
| PROTO-ONCOGENE PROTEINS C-KIT | PROTO-ONCOGENE PROTEIN C-KIT |
| PROTO-ONCOGENE PROTEINS C-MET | PROTO-ONCOGENE PROTEIN C-MET |
| PTEROYL POLYGLUTAMATE HYDROLASE | GAMMA-GLUTAMYL HYDROLASE |
| PUPILLARY FUNCTIONS, ABNORMAL | PUPIL DISORDERS |
| PYRUVATE CARBOXYLASE DEFICIENCY | PYRUVATE CARBOXYLASE DEFICIENCY DISEASE |
| PYRUVATE DEHYDROGENASE COMPLEX DEFICIENCY | PYRUVATE DEHYDROGENASE COMPLEX DEFICIENCY DISEASE |
| RADICULITIS | RADICULOPATHY |
| RECEPTORS, EPIDERMAL GROWTH FACTOR-UROGASTRONE | RECEPTOR, EPIDERMAL GROWTH FACTOR |
| RECEPTORS, INSULIN | RECEPTOR, INSULIN |
| RECEPTORS, INSULIN-LIKE-GROWTH FACTOR I | RECEPTOR, IGF TYPE 1 |
| RECEPTORS, INSULIN-LIKE-GROWTH-FACTOR II | RECEPTOR, IGF TYPE 2 |
| RECEPTORS, MACROPHAGE COLONY-STIMULATING FACTOR | RECEPTOR, MACROPHAGE COLONY-STIMULATING FACTOR |
| RECRUITMENT, LOUDNESS | HYPERACUSIS |
| REPTILASE | BATROXOBIN |
| RESTLESS LEGS | RESTLESS LEGS SYNDROME |
| RHIZOBIUM MELILOTI | SINORHIZOBIUM MELILOTI |
| RIBONUCLEOPROTEINS, SMALL, U1 | RIBONUCLEOPROTEIN, U1 SMALL NUCLEAR |
| RIBONUCLEOPROTEINS, SMALL, U2 | RIBONUCLEOPROTEIN, U2 SMALL NUCLEAR |
| RIBONUCLEOPROTEINS, SMALL, U4-U6 | RIBONUCLEOPROTEIN, U4-U6 SMALL NUCLEAR |
| RIBONUCLEOPROTEINS, SMALL, U5 | RIBONUCLEOPROTEIN, U5 SMALL NUCLEAR |
| SERINE PROTEINASES | SERINE ENDOPEPTIDASES |
| SINUS THROMBOSIS | SINUS THROMBOSIS, INTRACRANIAL |
| SPINOCEREBELLAR DEGENERATION | SPINOCEREBELLAR DEGENERATIONS |
| STIFF-MAN SYNDROME | STIFF-PERSON SYNDROME |
| SYMPTOMS AND GENERAL PATHOLOGY | PATHOLOGICAL CONDITIONS, SIGNS AND SYMPTOMS |
| TECHNOLOGY, MEDICAL LABORATORY | CLINICAL LABORATORY TECHNIQUES |
| ULNAR NERVE COMPRESSION SYNDROME | ULNAR NERVE COMPRESSION SYNDROMES |
| UROKINASE | URINARY PLASMINOGEN ACTIVATOR |
| VASCULAR HEADACHE | VASCULAR HEADACHES |
| VISION, SUBNORMAL | VISION, LOW |
| WALLENBERG'S SYNDROME | LATERAL MEDULLARY SYNDROME |
| WERDNIG-HOFFMANN DISEASE | SPINAL MUSCULAR ATROPHIES OF CHILDHOOD |
| APHASIA, WERNICKE | WERNICKE ENCEPHALOPATHY |
| ZENKER'S DIVERTICULUM | ZENKER DIVERTICULUM |
