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    Archived pages: 38 . Archive date: 2012-11.

  • Title: Linksamling til Nordisk information om sjældne handicap og kontaktmuligheder - Rarelink.dk
    Descriptive info: .. Vælg tilgængelighed.. |.. Gå til indhold.. Kun tekst.. :.. Høj kontrast.. Tekststørrelse:.. Linksamling til Nordisk information om sjældne handicap og kontaktmuligheder.. Vælg i alfabetisk diagnoseliste.. A.. B.. C.. D.. E.. F.. G.. H.. I.. J.. K.. L.. M.. N.. O.. P.. Q.. R.. S.. T.. U.. V.. W.. X.. Y.. Z.. Æ.. Ø.. Å.. 0-9.. Søg.. Diagnoselisten.. Her finder man links til information om sjældne handicap/diagnoser udarbejdet af offentligt anerkendte videnshavere på sjældne handicap området i Norge, Sverige, Finland og Danmark.. VIGTIGT: (oktober 2012).. Som følge af tekniske omlægninger i Danmark er linkene til de danske diagnosebeskrivelser midlertidigt ude af funktion.. Indtil det er ordnet, kan de  ...   personer/pårørende, der lever med samme sjældne handicap i Sverige, Norge, Finland og Danmark.. Kontakten kan enten foregå via patientforeningerne i de respektive lande eller via Den Danske Kontaktordning.. Ordningen gælder for personer i Danmark, Norge og Sverige, administreres i Danmark og er under dansk lovgivning.. For personer i Finland kan kontakten ske via den Finske Kontaktordning, som administreres i Finland og under finsk lovgivning.. Gå via alfabetet øverst på denne side og se mulighederne for kontakt ved hver enkelt diagnose.. Eller.. Få mere information her.. RSS feed for diagnoselisten.. (.. Hvad er RSS?.. ).. Støttet af Nordisk Ministerråd.. Hjem.. Hvad er rarelink?.. Dansk.. Norsk.. Svensk.. Engelsk.. Finsk.. Islandsk..

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  • Title: Vælg tilgængelighed - Rarelink.dk
    Descriptive info: Denne hjemmeside er i overensstemmelse med.. W3V WCAG-AA.. retningslinjerne.. For at lette navigeringen, findes der også genvejstaster til hovedmenupunkterne:.. Indhold.. Valg af tilgængelighed (denne side).. Kontakt.. Om rarelink.. De fleste Windows- og Linux-baserede internetbrugere skal trykke på Alt + genvejstasten - fx Alt+O - for å læse "Om rarelink".. Hos nogle internetbrugere kræver det, at skal man også trykker Enter til sidst.. Opera-brugere skal trykke Shift + Esc for å komme i genvejs-modus og dermed kunne trykke en genvej.. Mac-brugere skal  ...   Strict og CSS i overensstemmelse med W3c standard.. Siderne følger også retningslinier for tilgængelighed, således at indholdet er tilgængeligt for så mange som muligt.. Siden er udviklet i samarbejde med.. IxD.. , et design- og udviklingsbureau, specialiseret i brugervenlighed og tilgængelighed.. RSS.. RSS feeds giver dig mulighed for at følge med i opdateringerne på rarelink.. dk.. For at benytte RSS-feeds skal du have en RSS-læser, eller en browser, som understøtter dette (fx.. Firefox.. På.. Download.. com.. kan man gratis downloade forskellige RSS-læsere..

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  • Title: Diagnoselisten - Rarelink.dk
    Descriptive info: Grafisk version.. Vis diagnoselisten på følgende sprog:.. Alle sprog.. Diagnoser,.. Aagenaes syndrome.. (Engelsk).. Aagenæs syndrom.. (Dansk).. Aarskog syndrom.. Aarskog syndrome.. Abetalipoproteinaemi.. Abetalipoproteinemia.. ACC.. ACHM2.. Achondroplasi.. Achondroplasia.. Achromatopsia 2.. ACPS II.. Acrocephalopolysyndactyly type II.. Acrocephalosyndactyly type I.. Acrocephalosyndactyly type II.. Acute intermittent porphyria.. ADEM.. Adiposis dolorosa.. Adrenal Hyperplasia, Congenital, Due To 21-Hydroxylase Deficiency.. Adrenogenitalt syndrom.. Adrenoleukodystrofi.. Adrenoleukodystrophy.. Adrenoleukodystrophy, autosomal neonatal form.. Adrenomyeloneuropathy.. Adrenomyeloneuropati.. Adynamia episodica hereditaria.. Afibrinogenemia.. Afibrinogenæmi.. Agenesis of the corpus callosum.. Agnogenic myeloid metaplasia.. AHC.. Ahornsirup urin sygdom.. Aicardi syndrom.. Aicardi syndrome.. Aicardi-Goutieres syndrom.. Aicardi-Goutieres syndrome.. AIS.. Akromatopsi.. Akut dissemineret encefalomyelitis.. Akut intermitterende porfyri.. Akut polyradiculitis.. AL amyloidose.. Alagille s syndrome.. Alagilles syndrom.. Albinisme, Okulo-kutan.. Albinisme, Okulær.. Albright Hereditary Osteodystrophy.. Albrights hereditære osteodystrofi.. Alexander disease.. Alexander sygdom.. Alfa-1-antitrypsinmangel.. Alkaptonuri.. Alkaptonuria.. Allergic Angiitis and Granulomatosis.. Allergisk granulomatøs vasculitis.. ALMS.. Alpers diffuse degeneration of cerebral grey matter  ...   Androgen insensitivity syndrome.. Androgent insensitivitetssyndrom.. Anemia, Sideroblastic, X-Linked.. Angelman syndrom.. Angelman syndrome.. Angioedema, Hereditary.. Angioneurotic edema.. Angioødem, hereditært.. Aniridi.. Aniridi, cerebellar ataksi og udviklingshæmning.. Aniridia congenita.. Aniridia type II.. Aniridia, Cerebellar Ataxia, And Mental Deficiency.. Anorectal anomalies.. Antenatal Hydronephrosis.. Anti-fosfolipid antistofsyndrom.. Antiphospholipid Syndrome.. APECED syndrome.. Apert syndrom.. Apert syndrome.. Aplasia cutis congenita.. Apolipoprotein B deficiency.. Argininemia.. Argininoravsyreæmi.. Argininosuccinase Deficiency.. Argininosuccinicaciduria.. Argininravsyreuri.. Argininæmi.. Arnold-Chiari malformation.. Arnold-Chiaris malformation.. ARPKD.. Arspartylglykosaminuri.. Arteriohepatic dysplasia.. Arteriohepatisk dysplasi.. Arteriovenous malformation.. Arteriovenøse malformationer.. Arthrogryposis multiplex congenita.. Arthrogryposis Multiplex Congenita With Pulmonary Hypoplasia.. Arthroophthalmopathy, Hereditary Progressive.. Artrogryposis multiplex congenita.. Aspartylglycosaminuria.. Asphyxiating Thoracic Dystrophy.. asphyxiating thoracic dystrophy.. Ataxia telangiectasia.. Ataxia telangiektasia.. Atp synthetase deficiency.. ATP-syntase-mangel.. ATTR amyloidose.. Autoimmun lymfoproliferativt syndrom.. Autoimmun trombocytopenisk purpura.. Autoimmune lymphoproliferative syndrome.. Autoimmune polyendocrinopathy syndrome, type I.. Autoimmune thrombocytopenic purpura.. Autonomic Control, Congenital Failure Of.. Autosomal recessive polycystic kidney disease.. AVM.. Information..

    Original link path: /diagnoselist.jsp?capitalLetter=A&synonymsIncluded=true
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  • Title: Diagnoselisten - Rarelink.dk
    Descriptive info: Balo s concentric sclerosis.. Balós koncentriske sklerose.. Bardet-Biedl syndrom.. Bardet-Biedl syndrome.. Barraquer Simons syndrom.. Barraquer Simons Syndrome.. Bartter syndrom.. Bartter Syndrome.. Basal cell nevus syndrome.. Bassen-Kornzweig syndrom.. Bassen-Kornzweig syndrome.. Batten Disease.. Batten sygdom.. BBS.. Bean syndrom.. Bean syndrome.. Becker muscular dystrophy.. Beckers muskeldystrofi.. Beckers sygdom.. Beckwith-Wiedemann syndrom.. Beckwith-Wiedemann syndrome.. Behcet sygdom.. Behcet´s disease.. Behr syndrom.. Behr syndrome.. Benign intrakraniel  ...   Biliary atresia, extrahepatic.. Binyrebarkhyperplasi med 21-hydroxylasemangel, kongenit.. Biotinidase Deficiency.. Biotinidase mangel.. Bird-headed dwarfism.. Bird-Headed Dwarfism.. Bladder extrophy.. Bloch-Sulzberger syndrom.. Blue Rubber Bleb Naveus syndrom.. Blue Rubber Bleb Nevus.. Blæreektopi.. Blødersygdomme.. BMD.. BOR-syndrome.. Borjeson-Forssman-Lehmann syndrom.. Borjeson-Forssman-Lehmann syndrome.. BPP.. Branchiootorenal Dysplasia.. Brankio-oto-renalt syndrom.. Broad thumb-hallux syndrome.. Bruton agammaglobulinemia turosine kinase.. Bruton agammaglobulinæmi.. Bugvægsdefekt.. Bulldog Syndrome.. Bullous pemphigoid.. bulløs iktyosis.. Bulløst pemphigoid.. BWS..

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  • Title: Diagnoselisten - Rarelink.dk
    Descriptive info: CADASIL.. Caffey disease.. Caffey syndrom.. Campomel dysplasi.. Campomelic dysplasia.. Canavan disease.. Canavans sygdom.. Carbamoylphosphate Synthetase I Deficiency.. Carbohydrate Deficient Glycoprotein Syndrome.. Carbohydrate-deficient glycoprotein syndrome.. Cardio-facio-cutaneus syndrom.. Cardiofaciocutaneous Syndrome.. Cardiomyopathy, Dilated.. Carpenters syndrom.. Carpenters syndrome.. Cat eye syndrom.. Cat eye syndrome.. CATCH 22.. Caudal Dysplasia.. Caudal regression syndrome.. CBPS.. CCC syndrom.. CCD.. CCHS.. CDG.. CDG syndrom.. CDPXD.. Central Core Disease.. Central core disease of muscle.. Central hypoventilationssyndrom, kongenit.. Centronukleær myopati.. CEP.. Cephalocele.. Cerebellar hypoplasi.. Cerebellar hypoplasia.. Cerebelloparenchymal disorder IV.. Cerebral arteriopathy, autosomal dominant with subcortical infarcts and leukoencephalopathy.. Cerebral autosomal dominant arteriopati med subkortikale infarkter og leukoencefalopati.. Cerebral gigantism.. Cerebral gigantisme.. Cerebrohepatorenal syndrome.. Ceroid lipofuscinosis neuronal 1, infantile.. Ceroid lipofuscinosis neuronal 3, juvenile.. Ceroid lipofuscinosis, neuronal 1, infantil.. Cervical vertebral fusion.. Cervical vertebral fusion, autosomal recessive.. CF.. CFC syndrom.. CGD.. Charcot-Marie-Tooth Disease.. Charcot-Marie-Tooth sygdom.. CHARGE association.. CHARGE kompleks.. CHARGE syndrom.. Childhood disintegrative disorder.. CHLS.. Choanal atresi.. Choanal atresia.. Cholestase-lymfødem syndrom.. Cholestasis-lymphedema syndrome.. Chondrodysplasia punctata 2, X-bunden dominant.. Chondrodysplasia punctata 2, X-linked dominant.. Chondrodysplasia punctata, X-bunden recessiv.. Chondrodysplasia punctata, X-linked recessive.. Chondroectodermal dysplasia.. Christ-Siemens-Touraine syndrom..  ...   syndrome.. Cohen syndrom.. Cohen syndrome.. Colorblindness, Blue-Mono-Cone-Monochromatic Type.. Common variable immunodeficeincy.. Common variable immunodeficeincy, CVID.. Complex I deficiency.. Complex II deficiency.. Complex III deficiency.. Complex III, Cytochrome b Subunit.. Complex IV deficiency.. Complex V deficiency.. Congenital adrenal hyperplasia.. Congenital central hypoventilation syndrome.. Congenital claucoma.. Congenital Disorders of Glycosylation.. Congenital erythropoietic porphyria.. Congenital fiber type disproportion.. Congenital Hydronephrosis.. Congenital immune deficiency diseases.. Congenital limb deficiency.. Congenital melanocytic naevus.. Congenital muscular dystrophy.. Congenital ocular motor apraxia.. Conotruncal anomali face syndrom.. Conotruncal anomaly face syndrome.. CONRADI-HUNERMANN SYNDROME.. CONRADI-HUNERMANN-HAPPLE SYNDROME.. Conradi-Hünermann s sygdom.. Cornelia de Lange syndrom.. Cornelia de Lange syndrome.. Corpus callosum agenesi.. Corticobasal degeneration.. Costello syndrom.. Costello syndrome.. COX-mangel.. CPEO.. Craniocarpotarsal dystrophy.. Craniocarpotarsal Dystrophy.. Craniocerebellocardiac dysplasi.. Craniocerebellocardiac dysplasia.. Craniopharyngioma.. Cranium bifidum.. Creutzfeldt-Jakob disease.. Creutzfeldt-Jakob sygdom.. Cri du chat syndrom.. Cri-du-chat syndrome.. Crouzon syndrom.. Crouzon syndrome.. Cryopyrin associated periodic syndromes.. Cutaneous amyloidosis, primary.. Cutis marmorata telangiectatica congenita.. CVID.. Cystic angiomatosis of bone.. Cystic Angiomatosis Of Bone, Diffuse.. Cystic fibrosis.. Cystinose.. Cystinosis, Nephropathic.. Cystinuri.. Cystinuria.. Cystisk fibrose.. Cytochrom c-oxidase-mangel.. Cytochrome b of Complex III.. Cytochrome c oxidase deficiency..

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  • Title: Diagnoselisten - Rarelink.dk
    Descriptive info: D-vitamin resistent rhachitis.. Dancing eye syndrome.. Dandy-Walker malformation.. Dandy-Walker syndrom.. Dandy-Walker syndrome.. Dandy-Walker-like malformation atrioventricular septal defect.. Danon disease.. Danon sygdom.. Darier disease.. Darier s sygdom.. DDON.. De Morsier syndrom.. Deaf-blindness.. Deafness--Optic Atrophy Syndrome.. Deafness-dystonia-optic neuronopathy syndrome.. Deficiency of the mitochondrial respiratory chain complex I.. Deficiency of the mitochondrial respiratory chain complex II.. Deficiency of the mitochondrial respiratory chain complex IV.. Deficiency of the mitochondrial respiratory chain complex V.. Degeneratio hepatolenticularis.. Deletion 22q13  ...   insipidus.. Diamond Blackfan anemia.. Diamond-Blackfans anæmi.. Diamond-Blackfans syndrom.. Diastrophic dysplasia.. Diatrofik dysplasi.. DIDMOAD.. DiGeorge syndrom.. Dilateret cardiomyopati, familiær.. Dravet syndrome.. Dravets syndrom.. Duane Retraction syndrom.. Duane Retraction Syndrome.. Duane syndrom.. Dubin-Johnson syndrom.. Dubin-Johnson syndrome.. Dubowitz syndrom.. Dubowitz syndrome.. Duchenne muscular dystrophy.. Duchenne muskeldystrofi.. Duodenal atresia.. Duodenalatresi.. Dværgvækst.. Dwarfism.. Dyggve-Melchior-Clausen Disease.. Dyggve-Melchior-Clausen syndrom.. Dysmeli.. Dysplasia Gigantism Syndrome.. Dystonia musculorum deformans.. Dystonia Musculorum Deformans.. Dystonia-Parkinsonism, X-linked.. Dystrofia musculorum progressiva Duchenne.. Dystrophia myotonica.. Dystrophy myotonica.. Døvblindhed..

    Original link path: /diagnoselist.jsp?capitalLetter=D&synonymsIncluded=true
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  • Title: Diagnoselisten - Rarelink.dk
    Descriptive info: Eales disease.. Eales sygdom.. Ear, Patella, Short Stature Syndrome.. Ectodermal dysplasia 1,anhidrotic.. Ectodermal Dysplasia, Hypohidrotic.. Ectodermal Dysplasia, Hypohidrotic, with immune deficiency.. ED 1.. EDM1.. EDMD.. EDS.. EDS IV.. Edwards syndrom.. Ehlers-Danlos syndrom.. Ehlers-Danlos syndrome.. Ehlers-Danlos syndrome type IV, autosomal dominant.. Ehlers-Danlos syndrome, vascular type.. Ellis van Creveld syndrom.. Ellis-van Creveld syndrome.. Emanuel syndrom.. Emery-Dreifuss muscular  ...   Multiple.. Eosinofil gastroenteritis.. Eosinofil pneumoni.. Eosinophilic Granulomatous Vasculitis.. Epidermolysis bullosa.. Epidermolytic Hyperkeratosis.. Epilepsy, Progressive Myoclonus 1.. Epileptic encephalopathy, Lennox-Gastaut type.. Epiphysial dysplasia, multiple.. Episodic ataxia, type 1.. Episodic ataxia, type 2.. Episodisk ataksi, type 1.. Episodisk ataksi, type 2.. EPP.. Erythropoietic porphyria, congenital.. Erythropoietic protoporphyria.. Erytropoietisk protoporfyri.. EVC.. Exostoses, Multiple, Type I.. Extrahepatic biliary atresia..

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  • Title: Diagnoselisten - Rarelink.dk
    Descriptive info: Fabry disease.. Fabrys sygdom.. Facial hemispasm.. Facio-Auriculo-Vertebral Spectrum.. Facio-scapulo-humeral muskeldystrofi 1A.. Faciocutaneoskeletal syndrom.. Faciogenital dysplasi.. Faciogenital Dysplasia.. Facioscapulohumeral muscular dystrophy 1A.. Factor V deficiency.. Factor VII deficiency.. FADS.. Fahr disease.. Faktor V mangel.. Faktor VII mangel.. Familial mediterranean fever.. Familiær Hæmofagocytisk Lymfohistiocytose.. Familiær middelhavsfeber.. Familiær progressiv scleroderma.. Fanconi anemia.. Fanconis anæmi.. Farveblindhed, total.. FAV.. Fetal Akinesia Deformation Sequence.. Fetal Akinesia Sequence.. Fetal face  ...   dysplasi.. Fifth Digit Syndrome.. First and Second Branchial Arch Syndrome.. Floating-Harbor syndrome.. Focal Dermal Hypoplasia.. Fokal dermal hypoplasi.. FOP.. Fosfofruktokinasemangel.. Fragile Site Mental Retardation 1 Gene.. Fragile X Syndrome.. Fragilt X syndrom.. Francheschetti-Klein syndrom.. FRDA.. Freeman-Sheldon syndrom.. Freeman-Sheldon Syndrome.. Friedreich ataxia.. Friedreichs ataksi.. Frontonasal dysplasi.. Frontonasal dysplasia.. Fruktose intolerance, hereditær.. FSHMD1A.. Fucosidosis.. Fukosidose.. Fundus flavimaculatus.. Föllings sygdom.. Føtalt akinesi deformering sekvens.. Føtalt akinesi syndrom..

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  • Title: Diagnoselisten - Rarelink.dk
    Descriptive info: G Syndrome.. Galactosemia.. Galaktosæmi.. Galdevejsatresi.. Gamstorp sygdom.. Gastroenteritis, Eosinophilic.. Gastroschise.. Gastroschisis.. Gaucher disease type III.. Gauchers sygdom.. Giant pigmented hairy nevus.. Giant Platelet Syndrome.. Gilles de la Tourette syndrom.. Gilles de la Tourette syndrome.. Gillespie syndrom.. Gillespie syndrome.. Glanzmann og Naegeli thrombasthenia.. Globoid-celle leukodystrofi.. Glucosidase, acid, alpha deficiency.. Glutaracidemia I.. Glutaraciduria I.. Glutarsyreuri type 1.. Glycerol kinase deficiency..  ...   V.. Glycogen storage disease VII.. Glykogen storage disease type V.. Glykogenose type V.. Glykogenose type VII.. GM2-Gangliosidosis, TYPE II.. Golabi-Rosen syndrom.. Goldenhar syndrom.. Goldenhar syndrome.. Goldenhar-Gorlin Syndrom.. Goltz syndrom.. Goltz Syndrome.. Goltz-Gorlin syndrom.. Goltz-Gorlin Syndrome.. Gorham disease.. Gorham-Stout disease.. Gorham-Stout Disease.. Gorlin syndrom.. Gorlin syndrome.. Gorlin-Goltz syndrom.. GPHN.. Granulomatous disease, chronic.. Guillain-Barré syndrom.. Guillain-Barré syndrome.. Günter s disease..

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  • Title: Diagnoselisten - Rarelink.dk
    Descriptive info: Hairy naevus.. Hallermann-Streiff syndrom.. Hallermann-Streiff syndrome.. Hallervorden-Spatz Disease.. Hallervorden-Spatz sygdom.. Hand-Schüller-Christians sygdom.. Hartnup disease.. Hartnup disorder.. Hartnup syndrom.. HC.. HCP.. Hellers syndrom.. Hemifacial microsomi.. Hemifacial microsomia.. Hemihyperplasi.. Hemihyperplasia.. Hemihypertrofi.. Hemimegalencephaly.. Hemophagocytic Lymphohistiocytosis, Familial.. Hemophilia.. Hemophilia A.. Hemophilia B.. Hepatoerythropoietic porphyria.. Hepatorenal Tyrosinemia.. Hepatorenal tyrosinæmi.. Hereditary coproporphyria.. Hereditary fructose intolerance.. Hereditary multiple exostosis.. Hereditary myopathy with lactic acidosis.. Hereditary Progressive Arthroophthalmopathy.. Hereditary sensory and autonomic neuropathy type V.. Hereditary spastic paraplegia.. Hereditær fruktose intolerance.. Hereditær glomerulonephritis.. Hereditær hypokrom anæmi.. Hereditær motorisk sensorisk neuropati.. Hereditær spastisk paraparese.. Hereditær spastisk paraplegi.. Hereditær trykbetinget neuropati.. Hereditært angioødem.. Heredopathia atactica polyneuritiformis.. Herpes simplex encephalitis.. HES.. HFM.. Hirschsprung disease.. Hirschsprung disease - mental retardation syndrome.. Hirschsprungs sygdom..  ...   Syndrome.. Hurler-Scheie syndrom.. Hurler-Scheie syndrome.. Hurst syndrom.. Hutchinson-Gilford Progeria Syndrome; Hgps.. Hutchinson-Gilfords syndrom.. Hydrocephalus.. Hydrocephaly.. HYP.. Hyper-IgD syndrom.. Hyper-IgD Syndrome.. Hyper-IgE syndrom.. Hyper-IgE Syndrome.. Hyper-IgM syndrom.. Hyperammonemia due to Carbamoyl Phosphate Synthetase I Deficiency.. Hypereosinofilt syndrom.. Hypereosinophilic syndrome.. Hyperglycerolemia.. Hyperglycerolæmi.. Hyperinsulinism, congenital.. Hyperinsulinisme, kongenit.. Hyperkalemic periodic paralysis.. Hyperostosis Corticalis Deformans Juvenilis Hyperphosphatasemia.. Hyperostosis generalisata with striations.. Hyperostosis Generalisata With Striations.. Hyperoxaluria, Primary, Type I.. Hypertelorism with Esophageal Abnormality and Hypospadias.. Hypochondroplasia.. Hypofosfatasi.. Hypofosfatæmi, X-bunden.. Hypofosfatæmisk vitamin D resistent rhachitis.. Hypohidrotisk ectodermal dysplasi.. Hypohidrotisk ektodermal dysplasi med immundefekt.. Hypomelanosis of Ito.. Hypoparathyreoidisme, isoleret.. Hypoparathyroidism.. Hypophosphatasia.. Hypophosphatemia, X-linked.. Hypoplastic left heart syndrome.. Hypopospadias-dysphagia syndrome.. Hypotension, Orthostatic.. Hypoventilationssyndrom, kongenit central.. HYPP.. Hæmofili A.. Hæmofili B..

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  • Title: Diagnoselisten - Rarelink.dk
    Descriptive info: I-cell sygdom.. Ichthyosis.. Ichthyosis Bullosa Of Siemens.. Ichthyosis, Bullous Type.. Ichthyosis, Lamellar, 1.. Idiopathic pulmonary fibrosis.. Idiopathic thrombocytopenic purpura.. Idiopathic torsion dystonia.. Idiopathic Torsion Dystonia.. Idiopatisk basalganglie forkalkning.. Idiopatisk intracraniel hypertension.. Idiopatisk trombocytopenisk purpura.. IgA-defekt.. Iktyosis.. Immuno osseous dysplasia.. Immunocytom.. Immunodeficiency with hyper-IgM, type 1.. Immunoglobulin A Deficiency Susceptibility 1.. Immunoossøs dysplasi, Schimke type.. Inclusion Body Myositis.. Incontinentia pigmenti.. Infantil cortical hyperostose..  ...   Cortical Hyperostosis.. Infantile Spasm syndrome,x-linked.. Infantile spasmer.. Inflammatoriske tarmsygdomme i barndommen.. Inflammatory bowel diseases in childhood.. Intestinal pseudoobstruction.. Intestinal pseudoobstruktion.. Intracranial Hypertension, Idiopathic.. Inverted duplicated chromosome 15.. Inverted duplication (15).. IP.. IPEX.. IPEX syndrome.. IRD.. Isaac syndrom.. Isaac syndrome.. Isochromosome 18p syndrome.. Isodicentrisk kromosom 15.. Isokromosom 18p syndrom.. Isoleret bilateral choanal atresi.. Isoleret hypoparathyreoidisme.. Isovaleriansyreæmi.. Isovaleric Acid CoA Dehydrogenase Deficiency.. Isovalericacidemia.. ITP..

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    Archived pages: 38