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orphaentry | 97252 | Mega-cisterna magna
orphaentry | 97249 | Pontocerebellar hypoplasia type 3
orphaentry | 97279 | Insulinoma
orphaentry | 97278 | PPoma
orphaentry | 97275 | Encephalitis
orphaentry | 97285 | Thyroid lymphoma
orphaentry | 97283 | Somatostatinoma
orphaentry | 97282 | VIPoma
orphaentry | 97280 | Glucagonoma
orphaentry | 97289 | Thymic neuroendocrine tumor
orphaentry | 97290 | Familial papillary thyroid carcinoma with renal papillary neoplasia
orphaentry | 97286 | Carney-Stratakis syndrome
orphaentry | 97287 | Bronchial neuroendocrine tumor
orphaentry | 97293 | Rare benign ovarian tumor
orphaentry | 97295 | Furlong syndrome
orphaentry | 97292 | Cardiogenic shock
orphaentry | 97332 | Kienbock disease
orphaentry | 97335 | Osgood-Schlatter disease
orphaentry | 97297 | Bohring-Opitz syndrome
orphaentry | 97330 | Thoracic outlet syndrome
orphaentry | 97338 | Melanoma of soft tissue
orphaentry | 97339 | Dural sinus malformation
orphaentry | 97336 | Panner disease
orphaentry | 97337 | Sinding-Larsen-Johansson disease
orphaentry | 97341 | Persistent placoid maculopathy
orphaentry | 97340 | Hunter-McAlpine craniosynostosis
orphaentry | 97346 | ADan amyloidosis
orphaentry | 97345 | ABri amyloidosis
orphaentry | 97349 | Postencephalitic parkinsonism
orphaentry | 97352 | Pellagra
orphaentry | 97353 | Dementia pugilistica
orphaentry | 97360 | Robinow syndrome
orphaentry | 97355 | Caribbean parkinsonism
orphaentry | 97361 | Renal hypoplasia, unilateral
orphaentry | 97362 | Renal hypoplasia, bilateral
orphaentry | 97363 | Unilateral multicystic dysplastic kidney
orphaentry | 97364 | Bilateral multicystic dysplastic kidney
orphaentry | 97366 | Multiloculated renal cyst
orphaentry | 97367 | Renal tubular dysgenesis due to twin-twin transfusion
orphaentry | 97368 | Drug-related renal tubular dysgenesis
orphaentry | 97369 | Renal tubular dysgenesis of genetic origin
orphaentry | 97548 | Ivemark syndrome
orphaentry | 97552 | Steroid-sensitive nephrotic syndrome without renal biopsy
orphaentry | 97555 | Sporadic idiopathic steroid-resistant nephrotic syndrome with collapsing glomerulopathy
orphaentry | 97556 | Congenital and infantile nephrotic syndrome
orphaentry | 97560 | Primary membranous glomerulonephritis
orphaentry | 96183 | Maternal uniparental disomy of chromosome 9
orphaentry | 96182 | Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7
orphaentry | 96181 | Maternal uniparental disomy of chromosome 6
orphaentry | 96180 | Maternal uniparental disomy of chromosome 4
orphaentry | 96179 | Maternal uniparental disomy of chromosome 2
orphaentry | 96178 | Ring chromosome 16 syndrome
orphaentry | 96177 | Ring chromosome 15 syndrome
orphaentry | 96176 | Ring chromosome 13 syndrome
orphaentry | 96191 | Paternal uniparental disomy of chromosome 6
orphaentry | 96190 | Paternal uniparental disomy of chromosome 5
orphaentry | 96188 | Maternal uniparental disomy of chromosome 22
orphaentry | 96187 | Maternal uniparental disomy of chromosome 21
orphaentry | 96186 | Maternal uniparental disomy of chromosome 20
orphaentry | 96185 | Maternal uniparental disomy of chromosome 16
orphaentry | 96184 | Temple syndrome due to maternal uniparental disomy of chromosome 14
orphaentry | 96194 | Paternal uniparental disomy of chromosome 20
orphaentry | 96195 | Paternal uniparental disomy of chromosome 21
orphaentry | 96192 | Paternal uniparental disomy of chromosome 7
orphaentry | 96193 | Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11
orphaentry | 96256 | Somatotropic adenoma
orphaentry | 96253 | Cushing disease
orphaentry | 96201 | X small rings
orphaentry | 96321 | Polyploidy
orphaentry | 96269 | Isolated partial vaginal agenesis
orphaentry | 96264 | 49,XXXXY syndrome
orphaentry | 96263 | 48,XXXY syndrome
orphaentry | 96266 | Leydig cell hypoplasia due to partial LH resistance
orphaentry | 96265 | Leydig cell hypoplasia due to complete LH resistance
orphaentry | 96344 | Rare gynecologic or obstetric disease
orphaentry | 96346 | Anorectal malformation
orphaentry | 96325 | Isochromosome Y
orphaentry | 96334 | Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14
orphaentry | 96333 | Rare otorhinolaryngological malformation
orphaentry | 97120 | Distal arthrogryposis
orphaentry | 97214 | Eisenmenger syndrome
orphaentry | 96369 | Early-onset schizophrenia
orphaentry | 97234 | Glycogen storage disease due to phosphoglycerate mutase deficiency
orphaentry | 97238 | Rippling muscle disease
orphaentry | 97239 | Reducing body myopathy
orphaentry | 97240 | Zebra body myopathy
orphaentry | 97229 | Riboflavin transporter deficiency
orphaentry | 97230 | Solar urticaria
orphaentry | 97231 | Ligneous conjunctivitis
orphaentry | 97232 | Fingerprint body myopathy
orphaentry | 97978 | Rare endocrine disease
orphaentry | 98004 | Rare immune disease
orphaentry | 97992 | Rare hematologic disease
orphaentry | 98006 | Rare neurologic disease
orphaentry | 98010 | Infectious disease of the nervous system
orphaentry | 98033 | Rare neurologic disease with psychiatric involvement
orphaentry | 98036 | Rare otorhinolaryngologic disease
orphaentry | 98023 | Rare systemic or rheumatologic disease
orphaentry | 98022 | Rare headache
orphaentry | 98027 | Rare disease with odontological manifestation

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