Du er her: Forside / intranet / orphafolder

orphaentry | 63455 | Paraneoplastic pemphigus
orphaentry | 63443 | Rare epithelial tumor of stomach
orphaentry | 63446 | Acrocapitofemoral dysplasia
orphaentry | 63999 | IgG4-related mediastinitis
orphaentry | 63862 | Schisis association
orphaentry | 60040 | Megalencephaly-capillary malformation-polymicrogyria syndrome
orphaentry | 60039 | Pudendal neuralgia
orphaentry | 60041 | Congenital heart block
orphaentry | 60032 | Recurrent respiratory papillomatosis
orphaentry | 60033 | Idiopathic bronchiectasis
orphaentry | 59303 | Neonatal ichthyosis-sclerosing cholangitis syndrome
orphaentry | 59305 | Gestational trophoblastic neoplasm
orphaentry | 59306 | McLeod neuroacanthocytosis syndrome
orphaentry | 59298 | Schilder disease
orphaentry | 60015 | Enlarged parietal foramina
orphaentry | 60025 | Pulmonary alveolar microlithiasis
orphaentry | 60026 | Pulmonary nodular lymphoid hyperplasia
orphaentry | 60030 | Loeys-Dietz syndrome
orphaentry | 59315 | Rhombencephalosynapsis
orphaentry | 60014 | Argyria
orphaentry | 57777 | Cirrhotic cardiomyopathy
orphaentry | 57196 | Medial condensing osteitis of the clavicle
orphaentry | 57194 | Aseptic osteitis
orphaentry | 57146 | Rare hepatic disease
orphaentry | 57145 | SUNCT syndrome
orphaentry | 56970 | Human prion disease
orphaentry | 56965 | Progressive bulbar paralysis of childhood
orphaentry | 56425 | Cold agglutinin disease
orphaentry | 59181 | Sorsby pseudoinflammatory fundus dystrophy
orphaentry | 59135 | Laing early-onset distal myopathy
orphaentry | 58040 | Osteoblastoma
orphaentry | 58017 | Classic hairy cell leukemia
orphaentry | 57782 | Mazabraud syndrome
orphaentry | 55595 | Autosomal dominant limb-girdle muscular dystrophy type 1F
orphaentry | 55596 | Autosomal dominant limb-girdle muscular dystrophy type 1G
orphaentry | 54595 | Craniopharyngioma
orphaentry | 54368 | Sarcocystosis
orphaentry | 54370 | Primary membranoproliferative glomerulonephritis
orphaentry | 54272 | Hepatocellular adenoma
orphaentry | 56304 | Atelosteogenesis type II
orphaentry | 56305 | Atelosteogenesis type III
orphaentry | 56044 | Carcinoma of gallbladder and extrahepatic biliary tract
orphaentry | 55880 | Chondrosarcoma
orphaentry | 55881 | Adamantinoma
orphaentry | 55654 | Hypotrichosis simplex
orphaentry | 55655 | Pneumococcal meningitis
orphaentry | 79217 | Other metabolic disease with skin involvement
orphaentry | 79215 | Oligosaccharidosis
orphaentry | 79214 | Disorder of biogenic amine metabolism and transport
orphaentry | 79219 | Metabolic disease involving other neurotransmitter deficiency
orphaentry | 79207 | Disorder of lysosomal amino acid transport
orphaentry | 79213 | Mucopolysaccharidosis
orphaentry | 79212 | Mucolipidosis
orphaentry | 79211 | Combined hyperlipidemia
orphaentry | 79233 | Hypoxanthine guanine phosphoribosyltransferase partial deficiency
orphaentry | 79230 | Hemochromatosis type 2
orphaentry | 79237 | Galactokinase deficiency
orphaentry | 79234 | Crigler-Najjar syndrome type 1
orphaentry | 79235 | Crigler-Najjar syndrome type 2
orphaentry | 79224 | Disorder of purine or pyrimidine metabolism
orphaentry | 79225 | Sphingolipidosis
orphaentry | 79226 | Sterol metabolism disorder
orphaentry | 79183 | Disorder of ketolysis
orphaentry | 79185 | Disorder of ornithine or proline metabolism
orphaentry | 79187 | Disorder of peptide metabolism
orphaentry | 79186 | Disorder of pentose phosphate metabolism
orphaentry | 79189 | Peroxisome biogenesis disorder
orphaentry | 79188 | Peroxisomal beta-oxidation disorder
orphaentry | 79175 | Disorder of gamma-aminobutyric acid metabolism
orphaentry | 79174 | Disorder of fatty acid oxidation and ketone body metabolism
orphaentry | 79177 | Gluconeogenesis disorder
orphaentry | 79179 | Disorder of glycerol metabolism
orphaentry | 79178 | Glucose transport disorder
orphaentry | 79181 | Disorder of histidine metabolism
orphaentry | 79200 | Disorder of energy metabolism
orphaentry | 79201 | Glycogen storage disease
orphaentry | 79204 | Lipid storage disease
orphaentry | 79190 | Disorder of phenylalanin or tyrosine metabolism
orphaentry | 79191 | Disorder of purine metabolism
orphaentry | 79192 | Disorder of pyridoxine metabolism
orphaentry | 79193 | Disorder of pyrimidine metabolism
orphaentry | 79194 | Disorder of serine or glycine metabolism
orphaentry | 79195 | Sterol biosynthesis disorder
orphaentry | 79196 | Disorder of the gamma-glutamyl cycle
orphaentry | 79197 | Disorder of branched-chain amino acid metabolism
orphaentry | 79157 | 2-methylbutyryl-CoA dehydrogenase deficiency
orphaentry | 79156 | Seizures-intellectual disability due to hydroxylysinuria syndrome
orphaentry | 79155 | Hydroxykynureninuria
orphaentry | 79154 | 2-aminoadipic 2-oxoadipic aciduria
orphaentry | 79153 | Idiopathic trachyonychia
orphaentry | 79152 | Disseminated superficial actinic porokeratosis
orphaentry | 79151 | Acrokeratosis verruciformis of Hopf
orphaentry | 79150 | Linear and whorled nevoid hypermelanosis
orphaentry | 79149 | Dermochondrocorneal dystrophy
orphaentry | 79148 | Elastosis perforans serpiginosa
orphaentry | 79147 | Familial reactive perforating collagenosis
orphaentry | 79146 | Familial progressive hyperpigmentation
orphaentry | 79145 | Dowling-Degos disease
orphaentry | 79144 | Isolated congenital onychodysplasia
orphaentry | 79143 | Isolated congenital anonychia

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