Filtering
- Abdominal aorta aneurisme
- Metabolsk syndrom i abdominal fedme
- Abetalipoproteinemia
- Abrikosov's Tumor
- Absent T Lymphocytes
- Acanthocheilonemiasis
- Acanthocytosis
- Acanthosis Nigricans
- Achalasia
- Achondroplasia
- Acinic Cell Carcinoma
- Akustisk nevrom
- Acquired Fructose Intolerance
- Ervervet hemofili
- Ervervet Von Willebrands syndrom
- Acral Lentiginous Melanoma
- Akromegali
- Actinic Cheilitis
- Akutt artikulær revmatisme
- Acute Biphenotypic Leukemia
- Akutt spredt encefalomyelitt
- Acute Erythroblastic Leukemia
- Akutt erythroid leukemi
- Akutt graft versus verts sykdom
- Akutt intermitterende porfyri
- Akutt lymfoblastisk leukemi
- Acute Lymphoblastic Leukemia, Childhood
- Akutt megakaryoblastisk leukemi
- Akutt monoblastisk leukemi
- Akutt fjellsykdom
- Akutt myeloblastisk leukemi med modning
- Akutt myeloblastisk leukemi uten modning
- Acute Myelocytic Leukemia
- Acute Myeloid Leukemia, Adult
- Acute Myeloid Leukemia, Childhood
- Akutt myelomonocytisk leukemi
- Akutt ikke-lymfoblastisk leukemi
- Akutt promyelocytisk leukemi
- Akutt lungesviktsyndrom
- Addison's Disease
- Adeninfosforibosyltransferasemangel
- Adenokarsinom i lungene
- Adenokarsinom i vedlegget
- Adenoid cystisk karsinom
- Adenom i binyrene
- Adenomyose
- Adenosindeaminase-mangel
- Binyrekreft
- Adrenokortisk karsinom
- Adrenoleukodystrophy X-linked
- Adrenomyeloneuropati
- Voksen neuronal ceroid lipofuscinose
- Afibrinogenemia
- Aggressiv NK-celleleukemi
- Aicardi syndrom
- AIDS Demenskompleks
- AL-amyloidose
- Alagilles syndrom
- Albinisme
- Albrights arvelige osteodystrofi
- Alkaptonuria
- Allergisk bronkopulmonal aspergillose
- Alpha 1-antitrypsin Deficiency
- Alpha-Thalassemia
- Alport syndrom
- Alstromsyndrom
- Alternerende hemiplegia i barndommen
- Alveolar echinokokkose
- Alveolar myk del sarkom
- Alveolitt, ekstrinsisk allergisk
- Alzheimer Disease Familial
- Alzheimers sykdom type 2
- Amaurosis Fugax
- Amebiasis
- Amelogenesis Imperfecta
- Amyloid Neuropathy
- Amyloidose AA
- Amyloidosis Cerebral
- Amyotrofisk lateral sklerose
- Anal kreft
- Anaplastisk astrocytom
- Anaplastisk ependymom
- Anaplastisk storcellelymfom
- Anaplastisk oligoastrocytom
- Anaplastisk oligodendrogliom
- Anaplastic Plasmacytoma
- Ancylostomiasis
- Andersen-Tawil syndrom
- Anencephaly
- Angelman syndrom
- Angiofollicular Lymph Hyperplasia
- Angioimmunoblastisk lymfadenopati med dysproteinemi
- Angiomatous Lymphoid Hamartoma
- Aniridia
- Anodontia
- Anorectal Atresia
- Fremre uveitt
- Miltbrann
- Antifosfolipidsyndrom
- Antisosial personlighetsforstyrrelse
- Antisyntase-syndrom
- Aortakarktasjon
- Stenose i aortaklaffen
- Aftøs stomatitt
- Aplasia Cutis Congenita
- Aplastisk anemi
- Tilsynelatende overskudd av mineralokortikoid
- Apraxia
- Arachnoiditt
- Arginase mangel
- Argininosuccinic Aciduria
- Aromatic Amino Acid Decarboxylase Deficiency
- Arrhythmogenic Right Ventricular Dysplasia
- Arterial Calcification Due to CD73 Deficiency
- Arthrogryposis Multiplex Congenita
- Asbestose
- Ashermans syndrom
- Aspartylglykosaminuri
- Aspergillose
- Asphyxia Neonatorum
- Ataxia Telangiectasia
- Atrielt myxom, familiært
- Atrioventrikulær septaldefekt
- Dempet familiær adenomatøs polypose
- Atypisk hemolytisk uremisk syndrom
- Auditory Neuropathy
- Auditory Perceptual Disorder
- Autoimmun enteropati
- Autoimmun hemolytisk anemi
- Autoimmun hepatitt
- Autoimmun indre øre sykdom
- Autoimmunt lymfoproliferativt syndrom
- Autoimmun pankreatitt
- Autosomal dominerende delvis epilepsi med auditive egenskaper
- Autosomalt recessivt hyper IgE-syndrom
- Autosomal resessiv polycystisk nyresykdom
- B-celleprolymfocytisk leukemi
- B-cell Lymphomas
- Babesiose
- Bakteriell meningitt
- Balo Disease
- Balo's Concentric Sclerosis
- Bardet-Biedl syndrom
- Bare lymfocytt syndrom
- Bare lymfocytt syndrom 2
- Barraquer-Simons Syndrome
- Barth-syndrom
- Bartters syndrom
- Basalcellekreft, flere
- Basilar Migraine
- Batten Disease
- Becker muskeldystrofi
- Becker's Nevus
- Behcet's Disease
- Bell's Palsy
- Godartet paroksysmal posisjonell svimmelhet
- Berger Disease
- Beriberi
- Berylliose
- Beste Vitelliform Macular Dystrofi
- Beta-galaktosidase-1-mangel
- Beta-thalassemia
- Betlem myopati
- Gallekanalkreft
- Galdekreftkreft
- Biotinidasemangel
- Birdshot Chorioretinopathy
- Birt-Hogg-Dube-syndrom
- BK-virus nefropati
- Blastisk plasmacytoid dendritisk celle
- Blastoma
- Blastomycosis
- Blefarospasme
- Bloom-syndrom
- Bone Cancer
- Botulisme
- Bourneville Syndrome
- Bowens sykdom
- Brain Stem Glioma, Childhood
- Hjernetumor, voksen
- Hjernesvulst, barndom
- Brystkreft, Mann
- Brenner Tumor of Ovary
- Sprø hornhinnesyndrom
- Bronchiolitis Obliterans
- Bronchiolitis Obliterans Organizing Pneumonia
- Bronkopulmonal dysplasi
- Brown-Sequard syndrom
- Brucellose
- Brugada syndrom
- Budd-Chiari syndrom
- Buerger sykdom
- Bulløs Pemphigoid
- Burkitt lymfom
- Burnett Schwartz Berberian Syndrome
- Buruli magesår
- CADASIL
- Kalsifylaksi
- Camurati-Engelmann sykdom
- Canavan sykdom
- Capillary Hemangioblastoma
- Karbamoylfosfatsyntetase 1-mangel
- Karsinoid syndrom
- Karsinoid svulst
- Kardiospasme
- Carney Complex
- Carnitine Palmitoyltransferase 2-mangel
- Caroli sykdom
- Castleman's Disease
- Cat Scratch Disease
- Katastrofalt antifosfolipidsyndrom
- Central Centrifugal Cicatricial Alopecia
- Sentral kjernesykdom
- Central Nervous System Lymphoma, Primary
- Central Post-stroke Pain
- Sentral serøs korioretinopati
- Cerebellar Astrocytoma, barndom
- Cerebellar Degeneration
- Cerebral astrocytom, barndom
- Cerebral Cavernous Malformation
- Cerebral Palsy Spastic Diplegic
- Cerebral Palsy Spastic Hemiplegic
- Væskelekkasje i hjernen
- Cerebrotendinøs Xanthomatosis
- Ceroid Storage Disease
- Cervical Dystonia
- Cervikal intraepitelial neoplasi
- Chagas sykdom
- Chanarin-Dorfman syndrom
- Chandlers syndrom
- Charcot-Marie-Tooth Disease
- Charcot-Marie-Tooth Disease Type 1A
- Chediak-Higashi syndrom
- Cherubism
- Chiari Misdannelse Type 2
- Chikungunya
- BARNESyndrom
- Disintegrative Disorder i barndommen
- Barndomsskizofreni
- Kolesystitt
- Kolera
- Cholestasis, Progressive Familial Intrahepatic 3
- Kolesteatom
- Chondrocalcinosis 2
- Kondrosarkom
- Chordoma
- Chorea Minor
- Choreoacanthocytosis
- Koriocarcinoma
- Korioretinitt
- Choroid Plexus Carcinoma
- Choroideremia
- Koroiditt
- Kromofil nyrecellekarsinom
- Kromosomal triplisering
- Sletting av kromosom 17p
- Sletting av kromosom 5q
- Kronisk aktiv Epstein-Barr-virusinfeksjon
- Chronic Berylliosis
- Kronisk graft versus verts sykdom
- Kronisk granulomatøs sykdom
- Chronic Infantile Neurological Cutaneous Articular Syndrome
- Kronisk inflammatorisk demyeliniserende polyneuropati
- Kronisk lymfocytisk leukemi
- Kronisk myeloid leukemi
- Kronisk myelomonocytisk leukemi
- Kroniske myeloproliferative lidelser
- Kronisk neutrofil leukemi
- Churg Strauss Syndrome
- Chylothorax, medfødt
- Cicatricial Pemphigoid
- Citrullinemia Type I
- Classic Kaposi Sarcoma
- Clear Cell Renal Cell Carcinoma
- KLIPPERE
- Clostridium Difficile
- Clostridium Sordellii
- Klyngens hodepine
- COACH Syndrome
- Kullarbeiderens pneumokoniose
- Pels sykdom
- Koksidioidomykose
- Cockayne syndrom
- Cogan's Syndrome
- Cold Agglutinin Disease
- Cold Contact Urticaria
- Collagenous Colitis
- Samler kanalkreft
- Combined Malonic and Methylmalonic Aciduria
- Vanlig variabel immunsvikt
- Compartment Syndrome
- Komplett Atrioventricular Canal
- Complex Regional Pain Syndrome
- Cone-rod Dystrophy
- Dystrofi med kjeglestang 2
- Medfødt binyrebark hyperplasi
- Medfødt amegakaryocytisk trombocytopeni
- Congenital Antithrombin Deficiency
- Medfødt aplastisk anemi
- Medfødt sentral hypoventilasjonssyndrom
- Medfødt cytomegalovirus
- Medfødt diafragmatisk brokk
- Medfødt dyserythropoietisk anemi
- Medfødt dyserythropoietisk anemi Type 1
- Medfødt fiberforhold
- Medfødt hjerteblokk
- Medfødt hemolytisk anemi
- Medfødt leverfibrose
- Medfødt herpes simplex
- Medfødt hypotyreose
- Medfødt muskeldystrofi
- Medfødt muskeldystrofi Type 1A
- Congenital Porphyria
- Medfødt Torticollis
- Conn's Syndrome
- Conotruncal hjerte misdannelser
- Konverteringsforstyrrelse
- Koronararterie-aneurisme
- Kortikobasal degenerasjon
- Cowden syndrom
- Craniofacial Dystonia
- Kraniofrontonasal dysplasi
- Kraniofaryngiom
- Craniosynostosis
- CREST-syndrom
- Creutzfeldt-Jakobs sykdom
- Crouzon syndrom
- Kryoglobulinemi
- Cryopyrin-associated Periodic Syndrome
- Kryptokokkose
- Kryptogen organiserende lungebetennelse
- Kryptosporidiose
- Currarino Triad
- Cushing's Syndrome
- Kutan Lupus Erythematosus
- Kutan mastocytose
- Kutan sklerose
- Kutan T-celle lymfom
- Cutis Laxa
- Cyclic Vomiting Syndrome
- Cystisk adenomatoid misdannelse i lungene
- Cystisk fibrose
- Cystic Hygroma
- Cysticercosis
- Cystinose
- Cystinuria
- Cystosarcoma Phyllodes
- Cytomegalic Inclusion Disease
- Cytomegalovirus retinitt
- Dancing Eyes-dancing Feet Syndrome
- Darier sykdom
- Dendritic Cell, Monocyte, B Lymphocyte, and Natural Killer Lymphocyte Deficie...
- Dengue-feber
- Denys-Drash-syndrom
- Depersonalization Disorder
- Dermatofibroma
- Dermatofibrosarcoma Protuberans
- Dermatomyositis
- Desmoid svulst
- Desmoplastisk liten rundcelletumor
- Devic Disease
- Dextrocardia
- Di Guglielmos syndrom
- Diamond-Blackfan anemi
- Diaphyseal Medullary Stenosis With Malignant Fibrous Histiocytoma
- DICER1-relatert Pleuropulmonary Blastoma Cancer Predisposition Syndrome
- Diffus astrocytom
- Diffus magekreft
- Diffuse Scleroderma
- Diffuse Systemic Sclerosis
- Dihydroksyadeninuri
- Utvidet kardiomyopati
- Utvidet kardiomyopati med hypergonadotropisk hypogonadisme
- Difteri
- Dominant Ichthyosis Vulgaris
- Donnai-Barrow syndrom
- Dopamin Beta hydroksylase mangel
- Høyre ventrikkel med dobbelt utløp
- Dravetsyndrom
- Dubin-Johnsons syndrom
- Duchenne muskeldystrofi
- Duhring Brocq Disease
- Dysequilibrium syndrom
- Dysferlinopati
- Dyskeratosis Congenita
- Dyskinesia, Drug Induced
- Dystonia 11
- Dystonia 12
- Dystrofisk epidermolyse Bullosa
- Dystrofinopati
- Eales sykdom
- Eastern Equine Encefalitt
- Ebolavirus sykdom
- Ebstein's Anomaly
- Eccentrochondrodysplasia
- Eclampsia
- Ektodermal dysplasi
- Svangerskap utenfor livmoren
- Ehlers-Danlos syndrom
- Eisenmenger syndrom
- Valgfri mutisme
- Embryonal karsinom
- Endemisk Kaposi Sarcoma
- Endolymphatic Sac Tumor
- Endometrial stromal sarkom
- Endomyokardiell fibrose
- Forstørret vestibular akveduktsyndrom
- Enteropathy-associated T-cell Lymphoma
- Eosinophilia-myalgia Syndrome
- Eosinophilic Enteropathy
- Eosinofil fasciitt
- Ependymoblastoma
- Ependymoma
- Epidermodysplasi Verruciformis
- Epidermolyse Bullosa
- Epidermolyse Bullosa Acquisita
- Epidermolyse Bullosa Simplex
- Epilepsi Ungdomsfravær
- Epileptic Encephalopathy Lennox-Gastaut Type
- Episodisk ataksi
- Episodisk ataksi med nystagmus
- Epithelial-myoepithelial Carcinoma
- Epiteloid sarkom
- Erdheim-Chester sykdom
- Erysipelas
- Erytromelalgi
- Erythroplakia
- Erytropoietisk protoporphyria
- Esophageal Atresia
- Spiserørskreft
- Esophageal Varices
- Esotropia
- Essensiell trombocytemi
- Essensiell tremor
- Esthesioneuroblastoma
- Evans syndrom
- Ewing's Family of Tumors
- Ewing's Sarcoma
- Exercise Induced Anaphylaxis
- Eksfolierende dermatitt
- Blærens eksstrofi
- Extracranial Germ Cell Tumor, Childhood
- Ekstragonadal kjønnscelletumor
- Fabry sykdom
- Facioscapulohumeral muskeldystrofi
- Faktor VII-mangel
- Faktor X-mangel
- Faktor XIII-mangel
- Fallopian Tube Cancer
- Familial Adenomatous Polyposis
- Familial Cold Autoinflammatory Syndrome
- Familial kolorektal kreft
- Familiedysautonomi
- Familial encefalopati med organer som inkluderer neuroserpin
- Familial ekssudativ vitreoretinopati
- Familial HDL-mangel
- Familial hemiplegisk migrene
- Familial Hemiplegic Migraine Type 1
- Familial Hyperinsulinism
- Familial hypertrofisk kardiomyopati
- Familial Isolert Hyperparathyroidism
- Familial Isolert hypofyseadenom
- Familial Mediterranean Fever
- Familial prostatakreft
- Familial Thoracic Aortic Aneurysm and Dissection
- Familial Transthyretin Amyloidosis
- Fanconi anemi
- Fanconi Bickel Syndrome
- Fanconi Renotubular Syndrome
- Dødelig familiær søvnløshet
- Felty's Syndrome
- Fosteralkoholspektrumforstyrrelser
- Fetal Edema
- Fostermakrosomi
- Fibrinogenmangel, medfødt
- Fibrosarkom
- Fiberdysplasi
- Focal Dermal Hypoplasia
- Focal Dystonia
- Focal Facial Dermal Dysplasia
- Follikulært lymfom
- Formaldehyde Poisoning
- Fournier Gangrene
- Fragile X Syndrome
- Frambesia Tropica
- Fraser syndrom
- Frasier syndrom
- Freeman Sheldon syndrom
- Freys syndrom
- Friedreich Ataxia
- Frontotemporal demens
- Fryns syndrom
- Fukosidose
- Galaktorré-hyperprolaktinemi
- Galaktoseepimerasemangel
- Galactosemia
- Galaktosialidose
- Gall Bladder Cancer
- Ganglioglioma
- Gardners syndrom
- Gastrisk lymfom
- Gastro-enteropancreatic Neuroendocrine Tumor
- Gastrointestinale stromale svulster
- Gastroschisis
- Gauchers sykdom
- Gauchers sykdom type 1
- Gauchers sykdom type 2
- Gauchers sykdom type 3
- Gelatinous Ascites
- Genital Dwarfism
- Geographic Tongue
- Germinoma
- Svangerskapstrofoblastisk svulst
- Giant Axonal Neuropathy
- Giant Cell Arteritis
- Kjempecelle myokarditt
- Kjempepapillær konjunktivitt
- Gigantisme
- Gigantomastia
- Gitelman syndrom
- Glanzmann Trombasthenia
- Glaukom 3 Primær infantil B
- Glaukom, medfødt
- Glioblastom
- Glioma
- Gliomatose Cerebri
- Gliosarkom
- Glomerulonefritt
- Glucagonoma
- Glucagonoma Syndrome
- Glucocorticoid-remediable Aldosteronism
- Glukose-6-fosfat dehydrogenase mangel
- Glykogen lagringssykdom type 2
- Oppbevaring av glykogen type 3
- Lagring av glykogen type 4
- GM1 gangliosidose
- Gonadal Dysgenesis
- Granulocytopeni
- Granuloma Annulare
- Granulosa Cell Tumor of the Ovary
- Graves' Disease
- Grå blodplatesyndrom
- Griscellis syndrom
- Veksthormonmangel
- Guillain-Barre syndrom
- Gyratatrofi av choroid og retina
- Influensa
- Hailey-Hailey sykdom
- Hårcelle leukemi
- Hand-Schuller-Christian Disease
- Hansens sykdom
- Hantavirus lungesyndrom
- Hjertetumor
- Tungmetallforgiftning
- HELLP-syndrom
- Helminthiasis
- Hemangioblastoma
- Hemangioendoteliom
- Hemangiopericytoma
- Hemifacial Microsomia
- Hemiplegia
- Hemiplegic Migraine
- Hemoglobin C sykdom
- Hemoglobin SC sykdom
- Hemolytic Uremic Syndrome
- Hemophagocytic Lymphohistiocytosis
- Hemofili
- Hemophilia A, Acquired
- Hemophilia A, Congenital
- Hemofili B
- Hemofil artropati
- Hemorrhagic Fever
- Hemosiderose
- Henoch-Schonlein Purpura
- Heparin-indusert trombocytopeni
- Hepatisk encefalopati
- Hepatitt E
- Hepatoblastoma
- Hepatocellular Carcinoma (fibrolamellar Variant)
- Hepatocellular Carcinoma, Childhood
- Hepatorenal syndrom
- Arvelig amyloidose
- Arvelig angioødem
- Arvelig ataksi
- Arvelig koproporfyri
- Arvelig elliptocytose
- Arvelig fruktoseintoleranse
- Arvelig hemorragisk telangiectasia
- Hereditary Hyperuricemia
- Arvelige flere osteokondromer
- Hereditary Neuropathy With Liability to Pressure Palsy
- Arvelig pankreatitt
- Arvelig spastisk paraplegi
- Arvelig sfærocytose
- Hermansky-Pudlak syndrom
- Herpes Simplex encefalitt
- Herpes Zoster Ophthalmicus
- Herpetic Keratitis
- Heterotaxy
- Hirschsprung's Disease
- Hans buntakykardi
- Hodgkin lymfom
- Hodgkin Lymphoma, Childhood
- Holoprosencefali
- Homocysteinemia
- Homocystinuria
- Homolog sløsesykdom
- Hoyeraal Hreidarsson syndrom
- HTLV-1 assosiert myelopati / tropisk spastisk paraparesis
- Humant T-celle leukemivirus type 1
- Humant T-celle leukemivirus type 2
- Hunter-McAlpine Syndrome
- Huntington sykdom
- Hurthle Cell Thyroid Cancer
- Hydatidiform føflekk
- Hydatidose
- Hydrocephalus
- Hydrops Fetalis
- Hyper IgE-syndrom
- Hyper-IgD syndrom
- Hyperacusis
- Hyperadrenalisme
- Hypereosinofilt syndrom
- Hyperlipidemia Type 3
- Hyperlipoproteinemia Type 1
- Hyperlipoproteinemia Type 2
- Hyperlipoproteinemia Type 5
- Hyperparatyreoidisme, primær
- Overfølsomhet Vaskulitt
- Hypoadrenalism
- Hypoaldosteronisme
- Hypokondroplasi
- Hypocomplementemic Urticarial Vasculitis
- Hypohidrotisk ektodermal dysplasi
- Hypokalemisk periodisk lammelse
- Hypolipoproteinemia
- Hypomagnesemia Primary
- Hypomelanotic Disorder
- Hypoparathyroidism
- Hypopharyngeal kreft
- Hypofosfatasi
- Hypofosfatemiske raketter
- Hypopituitarisme
- Hypoplastisk venstre hjertesyndrom
- Hypoplastisk høyre hjertesyndrom
- Jeg cellesykdom
- IBIDS Syndrome
- Ichthyosis Linearis Circumflexa
- Ichthyosis Vulgaris
- Idiopathic Adolescent Scoliosis
- Idiopathic Myopathy
- Idiopatisk lungefibrose
- Idiopatisk lungehemosiderose
- Idiopathic Pulmonary Hypertension
- Idiopatisk trombocytopenisk purpura
- Immun trombocytopeni
- Immunmangel med Hyper IgM Type 1
- Inborn Amino Acid Metabolism Disorder
- Inkludering Kroppsmyopati 2
- Inklusjon Body Myositis
- Inkludering Konjunktivitt
- Incontinentia Pigmenti
- Indolent B-celle lymfom
- Infantil apné
- Infantil skoliose
- Infantil-utbrudd stigende arvelig spastisk lammelse
- Smittsom leddgikt
- Infektiøs endokarditt
- Inflammatorisk brystkreft
- Inflammatorisk myofibroblastisk svulst
- Insulinlignende vekstfaktor I-mangel
- Insulinom
- Intestinal Pseudo-obstruction
- Intracranial Arteriovenous Malformation
- Intrahepatic Cholangiocarcinoma
- Intrahepatic Cholestasis of Gravidity
- Intraokulært melanom
- Intrauterine Infections
- Intravenøs leiomyomatose
- Iridocorneal endotel syndrom
- Isaac's Syndrome
- Isolert ACTH-mangel
- Japansk encefalitt
- Jeunes syndrom
- Joubert syndrom
- Joubert syndrom med oculorenale anomalier
- Junctional Epidermolysis Bullosa
- Juvenil Dermatomyositis
- Juvenil Huntington sykdom
- Juvenil myelomonocytisk leukemi
- Juvenil myoklonisk epilepsi
- Juvenil osteoporose
- Juvenile Retinoschisis
- Kabukis syndrom
- Kallmanns syndrom
- Kallmann Syndrome 3
- Kaposiform hemangioendoteliom
- Kartageners syndrom
- Kawasaki Syndrome
- Kennedys sykdom
- Keratokonus
- Keratomalacia
- Keratose, Seborrheic
- Kernicterus
- Kidney Cancer
- Kikuchi sykdom
- Klatskin Tumor
- Klebsiella
- Klinefelters syndrom
- Klippel-Trenaunay syndrom
- Krabbe Leukodystrophy
- Krukenberg Carcinoma
- KSHV Inflammatory Cytokine Syndrome
- Lactate Dehydrogenase A Deficiency
- Lafora sykdom
- Lambert Eaton Myasthenic Syndrome
- Lamellar Iktyose
- Landau-Kleffner syndrom
- Langerhans cellehistiocytose
- Large B Cell Diffuse Lymphoma
- Large Granular Lymphocyte Leukemia
- Laron syndrom
- Laryngeal kreft
- Laryngeal Cleft
- Laryngeal papillomatose
- Laryngomalacia
- Lassueur-Graham-Little Syndrome
- LCAD-mangel
- LCHAD-mangel
- Leber medfødt amaurose
- Leber Congenital Amaurosis 2
- Leber arvelig optisk nevropati
- Leber Miliary Aneurysm
- Venstre ventrikulær ikke-komprimering
- Legg-Calve-Perthes sykdom
- Legionellose
- Leigh syndrom
- Leiner sykdom
- Leiomyomatosis and Renal Cell Cancer, Hereditary
- Leiomyosarkom
- Leishmaniasis
- Lentigo Maligna melanom
- Leptospirose
- Lesch Nyhan Syndrome
- Leukemia, B-cell, Chronic
- Leukemi, myeloid
- Leukemi, T-celle, kronisk
- Leukodystrofi
- Leukomalacia
- Leukoplakia
- Levator syndrom
- Lewy Body Dementia
- Li-Fraumeni syndrom
- Lichen Planus Follicularis
- Lichen Sclerosus
- Liddle syndrom
- Lettkjededeposisjonssykdom
- Lembelte Muskeldystrofi
- Limb-girdle Muscular Dystrophy Type 2H
- Limb-girdle Muscular Dystrophy, Type 2A
- Limb-girdle Muscular Dystrophy, Type 2B
- Lembelte Muskeldystrofi, Type 2C
- Limbisk encefalitt
- Leppe- og munnhulekreft
- Lipodystrofi
- Lipogranulomatose
- Liposarkom
- Listeriainfeksjon
- Liver Cancer
- Lokalisert sklerodermi
- Innelåst syndrom
- Loeys-Dietz syndrom
- Logopenisk progressiv afasi
- Loiasis
- Langt QT-syndrom 1
- Lowe Oculocerebrorenal Syndrome
- Lupus nefritt
- Lymfeknute Neoplasma
- Lymfangiectasis
- Lymfangioleiomyomatose
- Lymfangiom
- Lymfangiomatose
- Lymfatisk filariasis
- Lymfoblastisk lymfom
- Lymphocytic Colitis
- Lymphoma AIDSrelated
- Lymphoma, Large-cell
- Lymphoma, Large-cell, Immunoblastic
- Lymphoma, Small Cleaved-cell, Diffuse
- Lymphoma, Small Cleaved-cell, Follicular
- Lymfomatoid granulomatose
- Lymfomatoid papulose
- Lymfomatøs thyroiditt
- Lymfosarkom
- Lynch Syndrome
- Malaria
- Malignant Fibrous Histiocytoma
- Ondartet kjønnscelletumor
- Ondartet hypertermi
- Malignant Mesenchymal Tumor
- Ondartet mesoteliom
- Ondartet blandet Mullerian svulst
- Ondartet perifer nerveskjoldtumor
- Malonyl-CoA Decarboxylase Deficiency
- Mansonelliasis
- Mantelcelle lymfom
- Urinsykdom av lønnesirup
- Marburg hemorragisk feber
- Marfans syndrom
- Mastocytose
- Maternell hyperfenylalaninemi
- Modenhetsdebut Diabetes of the Young
- McCune Albright Syndrome
- Meslinger
- Meckelsyndrom
- Meconium Aspiration Syndrome
- Medullary Cystic Kidney Disease
- Medulloblastom
- Medulloblastoma, barndom
- Melanoma, Familial
- Meliodosis
- Membranoproliferative Glomerulonephritis Type 2
- Membranøs nefropati
- Menetrier sykdom
- Meningioma
- Meningococcal Infection
- Meningokokkemi
- Menkes sykdom
- Kvikksølvforgiftning
- Merkel cellekreft
- Metakromatisk leukodystrofi
- Metastatisk plateepitelnakkekreft med okkult primær
- Metionin-adenosyltransferasemangel
- Methylmalonic Acidemia
- Mevalonic Aciduria
- Mikrocefali
- Mikroencefali
- Mikroskopisk polyangiitt
- Mikrosporidiose
- Midtlinje dødelig granulom
- Miller-Fisher Syndrome
- Milroy sykdom
- Minimal endringssykdom
- Mitokondrie Neurogastrointestinal Encefalopati Syndrome
- Mitokondriell trifunksjonell proteinmangel
- Blandet bindevevssykdom
- Miyoshi myopati
- Moebius Syndrome
- Molybden kofaktormangel
- Mondini dysplasi
- Mondor Disease
- Monkeypox
- Monoklonal gammopati av ubestemt betydning
- Montefiore Syndrome
- Morphea
- Morquio Syndrome A
- Morvan's Fibrillary Chorea
- Motor Neuro-ophthalmic Disorders
- Moyamoya sykdom
- Muckle-Wells syndrom
- Mukoepidermoid karsinom
- Mucopolysaccharidosis
- Mukopolysakkaridose Type I
- Mukopolysakkaridose Type II
- Mukopolysakkaridose Type III
- Mukopolysakkaridose Type IIIA
- Mukopolysakkaridose Type IIIB
- Mukopolysakkaridose Type VI
- Mukopolysakkaridose Type VII
- Muenke syndrom
- Multicentric Castlemans Disease
- Multicore sykdom
- Multifokal koroiditt
- Multifokal lymfangioendoteliomatose med trombocytopeni
- Multipel endokrin neoplasi type 1
- Multipel endokrin neoplasi type 2
- Multiple Endocrine Neoplasia Type 2A
- Multiple Endocrine Neoplasia Type 2B
- Multippelt myelom
- Flere systematrofi
- Multiple System Atrophy (MSA) With Orthostatic Hypotension
- Kusma
- Muscle Eye Brain Disease
- Muscular Dystrophy
- Myasthenia Gravis
- Mycobacterium Abscessus
- Mycobacterium Avium Complex
- Mycobacterium Xenopi
- Mycoplasmal lungebetennelse
- Mycosis Fungoides
- Myelitt
- Myelodysplastiske syndromer
- Myelodysplastisk / myeloproliferativ sykdom
- Myelofibrosis
- Myelomeningocele
- MYH9 Relatert trombocytopeni
- Myokarditt
- Myoklonus epilepsi
- Myopati Medfødt
- Myotonia Atrophica
- Myotonisk dystrofi
- Myoton Dystrofi Type 1
- Myotubular Myopathy
- Myxoid liposarkom
- Myxopapillary Ependymoma
- N-acetylglutamate Synthetase Deficiency
- Nail Patella Syndrome
- Narkolepsi
- Nasopharyngeal Carcinoma
- Nekrotiserende enterokolitt
- Nekrotiserende fasciitt
- Neisseria Meningitidis-infeksjon
- Nelson syndrom
- Neonatal herpes
- Neonatal Hypothyroidism
- Neonatal meningitt
- Neonatal ovariecyst
- Neonatal hjerneslag
- Neonatal systemisk lupus erythematosus
- Nephrocalcinosis
- Nefrogen diabetes Insipidus
- Nefrogen systemisk fibrose
- Nephropathic Cystinosis
- Nefrosklerose
- Nerve Sheath Neoplasm
- Nethertons syndrom
- Neuroacanthocytosis
- Neuroblastom
- Neuroepithelioma
- Nevrofibroma
- Neurofibromatosis
- Nevrofibromatose Type 1
- Nevrofibromatose Type 2
- Nevrofibrosarkom
- Neurogenic Diabetes Insipidus
- Malignt neuroleptisk syndrom
- Neuromyelitt Optica Spectrum Disorder
- Neuronal Ceroid Lipofuscinoses
- Neuropathy Hereditary Sensory and Autonomic Type 1
- Nevrosyfilis
- Nevrotoksisitetssyndrom
- Neutral Lipid Storage Disease With Myopathy
- Nevoid Basal Cell Carcinoma Syndrome
- Ny daglig vedvarende hodepine
- Niemann-Pick Disease
- Niemann-Pick sykdom type B
- Niemann-Pick sykdom type C1
- Nodulært melanom
- Nodulær regenerativ hyperplasi
- Ikke 24-timers søvnvåpenlidelse
- Non-Hodgkin Lymphoma, Childhood
- Nonalcoholic Steatohepatitis
- Ikke-medfødt medfødt Ichthyosiform erytroderma
- Nondystrofisk myotonia
- Ikke-feminin kjønnscelletumor
- Noonans syndrom
- Noonan Syndrome 1
- Norrie sykdom
- Notalgia Paresthetica
- Occipital Horn Syndrome
- Ochronosis
- Ocular Cicatricial Pemphigoid
- Okulært melanom
- Ocular Motility Disorders
- Okulær toksoplasmose
- Okulokutan albinisme
- Oculodentodigital Dysplasia
- Oculomotor Apraxia Cogan Type
- Oculopharyngeal muskeldystrofi
- Oligoastrocytom
- Oligodendroglioma
- Omenn syndrom
- Onchocerciasis
- Onkogen osteomalasi
- Optisk atrofi 1
- Optisk nevritt
- Optic Neuropathy, Anterior Ischemic
- Optic Pathway Glioma
- Oral kreft
- Oral leukoplakia
- Oral Lichen Planus
- Oralt plateepitelkarsinom
- Orbital lymfom
- Organic Acidemia
- Ornitin transkarbamylase mangel
- Orofaciodigital syndromer
- Orofaryngeal kreft, voksen
- Osteochondritis Dissecans
- Osteochondroma
- Osteogenesis Imperfecta
- Osteomalacia
- Osteomyelitt
- Osteopetrose
- Osteoporose-pseudogliomasyndrom
- Osteosarkom
- Oto-Palatal-digitalt syndrom
- Oto-palato-digitalt syndrom Type 1
- Eggstokkreft
- Ovarian Carcinosarcoma
- Ovarial Epithelial Cancer
- Ovariecimcelletumor
- Ovarial lav malign potensiell svulst
- Pachyonychia Congenita
- Paget sykdom, ekstramammar
- Palatopharyngeal inkompetens
- Pallister-Hall-syndrom
- Palmoplantar Keratoderma
- Bukspyttkjertelen adenom
- Bukspyttkjertelkreft
- Pancreatic Carcinoma, Familial
- Pancreatic Islet Cell Tumors
- PANDAS
- Pantothenate Kinase-associated Neurodegeneration
- Panuveitt
- Papillær nyrecellekreft
- Papilledema
- Papillon Lefevre syndrom
- Paragangliomas 1
- Parainfluenza Virus Type 3
- Paramyotonia Congenita
- Paraplegi
- Parapsoriasis
- Parathyroid karsinom
- Parkes Webers syndrom
- Paroksysmal nattlig hemoglobinuri
- Paroksysmal ventrikulær fibrillering
- Pars Planitis
- Patent Ductus Arteriosus
- Pearson syndrom
- Pectus Carinatum
- Pediatric Crohns Disease
- Pediatrisk multippel sklerose
- Pediatrisk ulcerøs kolitt
- Pelizaeus-Merzbacher sykdom
- Pemphigus
- Pemphigus Vulgaris
- Penis Agenesis
- Pentalogy of Cantrell
- Periarteritis Nodosa
- Periodic Fever, Familial, Autosomal Dominant
- Peripartum kardiomyopati
- Perifert T-celle lymfom
- Periventrikulær leukomalacia
- Peroxisome Biogenesis Disorders
- Vedvarende Truncus Arteriosus
- Peutz Jeghers Syndrome
- Peyronie Disease
- Pfeiffer syndrom
- PHACE-syndrom
- Phenylketonuria
- Feokromocytom
- Fosfoglyserat Kinase-mangel
- Lysfølsom epilepsi
- Pick's Disease
- Piebaldisme
- Pierre Robin Sequence
- Pigment-dispersjons syndrom
- Pigmentary Retinopathy
- Pigmentert villonodulær synovitt
- Pilocytisk astrocytom
- Pilomatrixoma
- Pineoblastom
- Pineoblastoma, Childhood
- Pineocytoma
- Piriformis syndrom
- Pityriasis Rubra Pilaris
- Plagiocefali
- Plasma celle leukemi
- Plasma Thromboplastin Antecedent Deficiency
- Mangel på blodplatelagringsbasseng
- Pleomorphic Malignant Fibrous Histiocytoma
- Pleomorfisk Xanthoastrocytoma
- Pleuropulmonal blastoma
- Pneumocystose
- Pneumonia, Eosinophilic
- Dikt syndrom
- Poliomyelitt
- Polyarteritt Nodosa
- Polyartikulær debut juvenil idiopatisk leddgikt
- Polycystisk leversykdom
- Polycytemia Vera
- Polydactyly
- Polyembryom
- Polymorphic Catecholergic Ventricular Tachycardia
- Polymyositis
- Polyomavirus Allograft nefropati
- Porencephaly
- Porokeratose av Mibelli
- Porphyria
- Porphyria Cutanea Tarda
- Post polio syndrom
- Post-transplantasjon lymfoproliferativ sykdom
- Posttraumatisk epilepsi
- Bakre urinrørsventiler
- Posterior uveitt
- Postural ortostatisk takykardisyndrom
- Prader-Willi syndrom
- Forgjengelig pubertet
- Premature Ovarian Failure, Familial
- Priapisme
- Primær agammaglobulinemi
- Primary Biliary Cirrhosis
- Primær karnitinmangel
- Primær ciliær dyskinesi
- Primær effusjonslymfom
- Primær hyperoksaluri type 1
- Primær lateral sklerose
- Primær pigmentert nodulær adrenokortisk sykdom
- Primær progressiv afasi
- Primær skleroserende kolangitt
- Prinzmetals variant Angina
- Progeria
- Progressiv hemifacial atrofi
- Progressiv multifokal leukoencefalopati
- Progressiv myoklonisk epilepsi
- Progressiv ikke-flytende afasi
- Progressiv supranukleær parese
- Prolactinoma, Familial
- Propionsyreemia
- Proteus syndrom
- Protoporphyria
- Prurigo Nodularis
- Pseudo-Turner Syndrome
- Pseudokolinesterase-mangel
- Pseudohypoparathyroidism
- Pseudohypoparathyroidism Type 1A
- Pseudomyotonia
- Pseudomyxoma Peritonei
- Pseudopelade av Brocq
- Pseudopseudohypoparathyroidism
- Pseudotumor Cerebri
- Pseudoxanthoma Elasticum
- Pterygium av konjunktiva og hornhinne
- Pudendal Neuralgia
- Pulmonal arteriovenøs misdannelse
- Lungødem av fjellklatrere
- Pulmonal surfactant Protein B, Mangel på
- Lungeventilenose
- Lung venestenose
- Pulmonary Venoocclusive Disease
- Pulmonal venøs returanomali
- Pulmonal stenose
- Punctate Inner Choroidopathy
- Ren autonom feil
- Ren rødcelleplasi
- Pyoderma Gangrenosum
- Pyridoksinmangel
- Pyropoikilocytosis Arvelig
- Q Feber
- Rabies
- Strålingsinducert brachial pleksopati
- Stråleindusert kreft
- Rasmussen Encefalitt
- Reaktiv artritt
- Rectal Neoplasm
- Gjentatt respiratorisk papillomatose
- Refsumsykdom
- Refsumsykdom, infantil form
- Tilbakevendende polykondritt
- Renal Cancer
- Renal Glycosuria
- Nyretubulær acidose
- Renal Tubular Acidosis, Distal, Autosomal Dominant
- Renal Tubular Dysgenesis
- Åndedrettssyndrom, spedbarn
- Restless Legs Syndrome, Susceptibility To, 6
- Retikulær dysgenese
- Retinitt Pigmentosa
- Retinitis Pigmentosa-deafness Syndrome
- Retinoblastom
- Retinopati av prematuritet
- Retroperitoneal fibrose
- Rett syndrom
- Revesz syndrom
- Rhabdoid svulst
- Rhabdomyosarcoma Alveolar
- Rhabdomyosarcoma Embryonal
- Revmatisk feber
- Richters syndrom
- Rickets
- Rod Myopathy
- Rothmund Thomson Syndrome
- Roussy Levy syndrom
- Rubella
- Rubinstein-Taybi syndrom
- Russell-Silver-syndrom
- Sacrococcygeal Teratom
- Sandhoff sykdom
- SAPHO-syndrom
- Sarkoidose
- Scheuermann sykdom
- Schistosomiasis
- Schwannoma
- Scleroatonic Muscular Dystrophy
- Scott syndrom
- Skjørbuk
- Selective IgA Deficiency
- Semantisk demens
- Seminom
- Senior Loken Syndrome
- Sensory Neuropathy Type 1
- Septo-optic Dysplasia
- Serpiginous choroiditt
- Sertoli-leydig Cell Tumors
- Alvorlig akutt luftveissyndrom
- Alvorlig kombinert immunsvikt
- Sezary syndrom
- Sharp Syndrome
- Shigellose
- Kort tarmsyndrom
- Shprintzen-Goldberg Craniosynostosis Syndrome
- Shwachman-Diamond syndrom
- Sialadenitt
- Sigdcelleanemi
- Sideroblastisk anemi Pyridoksin-ildfast autosomal resessiv
- Siderose
- Silikose
- Enkelt ventrikulært hjerte
- Sinonasal udifferensiert karsinom
- Sitosterolemi
- Situs Inversus
- Tynntarmskreft
- Small Non-cleaved Cell Lymphoma
- Kopper
- Smith-Magenis syndrom
- Soft Tissue Sarcoma
- Somatostatinom
- Krampaktig dysfoni
- Spastisk paraparesis
- Spastic Paraplegia Epilepsy Mental Retardation
- Sfæroid kroppsmyopati
- Sphingolipidosis
- Spielmeyer-Vogt Disease
- Spina Bifida
- Spinal Cord Neoplasm
- Spinal Muscle Atrophy
- Spinal Muscle Atrophy 1
- Spinal Muskular Atrophy Type 2
- Spinal Sjokk
- Spinocerebellar Ataxia
- Spinocerebellar Ataxia 1
- Spinocerebellar Ataxia 10
- Spinocerebellar Ataxia 2
- Spinocerebellar Ataxia 3
- Spinocerebellar Ataxia Type 6
- Splenomegali
- Spondylarthropathy
- Spontan koronararteriedisseksjon
- Sporotrichosis
- Squamous Cell Carcinoma of the Head and Neck
- Stargardt sykdom
- Status Epilepticus
- Stevens-Johnsons syndrom
- Stickler-syndrom
- Stiff Person Syndrome
- Still's Disease Adult Onset
- Stomach Carcinoma
- Streptokokkgruppe A Invasiv sykdom
- Stress Cardiomyopathy
- Strongyloidiasis
- Sturge-Webers syndrom
- Subkutan Pannikulitt-lignende T-celle lymfom
- Subependymal gigantcelle astrocytom
- Subependymoma
- Succinic Semialdehyde Dehydrogenase Deficiency
- Krybbedød
- Sulfittoksidase mangel
- Overfladisk spredning av melanom
- Superior limbisk keratokonjunktivitt
- Superior Vena Cava syndrom
- Supraglottisk kreft i strupehodet
- Supratentorial Primitive Neuroectodermal Tumor
- Supratentorial Primitive Neuroectodermal Tumors, Childhood
- Supravalvular Aorta Stenosis
- Susac syndrom
- Sydenhams Chorea
- Synovial sarkom
- Synovitt
- Syringomyelia
- Systemisk candidiasis
- Systemisk kapillærlekkasjesyndrom
- Systemisk mastocytose
- Systemisk debut ungdomsidiopatisk leddgikt
- T-Lymphocytopenia
- Takayasu arteritt
- Talipes Equinovarus
- Tanger sykdom
- Tay Sachs Disease
- Testicular Cancer
- Testotoksikose
- Stivkrampe
- Tetrahydrobiopterinmangel
- Tetralogy of Fallot
- Thalassemia
- Thoracic Outlet Syndrome
- Trombasthenia
- Trombotisk trombocytopen purpura, ervervet
- Thrombotic Thrombocytopenic Purpura, Congenital
- Thymic Epithelial Tumor
- Thyroid Cancer, Anaplastic
- Skjoldbruskkreft, follikulær
- Skjoldbruskkreft, Medullary
- Tyrotoksisk periodisk lammelse
- Flåttbåren encefalitt
- Tungekreft
- Toni-Debre-Fanconi Syndrome
- Toxic Epidermal Necrolysis
- Toxocariasis
- Trakeobronchomalacia
- Tracheoesophageal Fistula
- Trachoma
- Overgangscellekreft
- Transposisjon av de store arteriene
- Tverrgående myelitt
- Tremor Arvelig Essential, 1
- Treponema-infeksjon
- Trikotillomani
- Trichuriasis
- Tricuspid Atresia
- Trigeminal nevralgi
- Trigger Thumb
- Trisomi 13
- Trisomi 18
- Tropisk gran
- Trypanosomiasis, øst-afrikansk menneske
- Tuberkulose
- Tuberkuløs meningitt
- Tuberøs sklerose
- Tubular Aggregate Myopathy
- Tufted angioma
- Tufting Enteropati
- Harepest
- Turners syndrom
- Twin Twin Transfusion Syndrome
- Tylosis
- Tyfoidfeber
- Typhus
- Tyrosinemia Type 1
- Ulcerøs proktitt
- Unverricht-Lundborg sykdom
- Urakalkreft
- Urea syklusforstyrrelser
- Urinrørskreft
- Usher Syndrome
- Usher Syndrome Type 3
- Usher syndrom, type 1
- Usual Interstitial Pneumonia
- Uterine Sarcoma
- Uveal sykdommer
- VACTERL Association
- Vaginal kreft
- Variegate Porphyria
- Venezuelansk equine encefalitt
- Ventrikulære septaldefekter
- Vernal keratokonjunktivitt
- Vertical Talus, Congenital
- Viral hemorragisk feber
- Virusassosiert hemofagocytisk syndrom
- Visceral steatose
- VLCAD-mangel
- Vogt-Koyanagi-Harada Syndrome
- Von Hippel-Lindau Syndrome
- Vulvar kreft
- Vulvar Vestibulitis Syndrome
- WAGR-syndrom
- Waldenstrom makroglobulinemi
- Walker-Warburg syndrom
- Varmt antistoff hemolytisk anemi
- Vannmelon mage
- Watson Syndrome
- WDHA-syndrom
- Webers syndrom
- Wegener's Granulomatosis
- Wells syndrom
- Werner's Syndrome
- Wernicke-Korsakoff syndrom
- West Nile Encephalitis
- West Nile Virus
- Vestsyndrom
- Western Equine Encefalitt
- WHIM-syndrom
- Kikhoste
- Williams syndrom
- Wilms' Tumor
- Wilsons sykdom
- Wiskott Aldrich Syndrome
- Wolff-Parkinson-White Syndrome
- Wolfram syndrom
- Wolman sykdom
- X-bundet Adrenal Hypoplasia Congenita
- X-bundet Agammaglobulinemia
- X-bundet medfødt stasjonær nattblindhet
- X-bundet hypohidrotisk ektodermal dysplasi
- X-linked Ichthyosis
- X-bundet lymfoproliferativt syndrom
- X-linked Mental Retardation and Macro-orchidism
- X-bundet alvorlig kombinert immunsvikt
- Xeroderma Pigmentosum
- Gul feber
- Yolk Sac Tumor
- Zellwegers syndrom
- Zollinger-Ellisons syndrom
- Zygomycosis
- 21-hydroksylase mangel
- 22q11.2 Slettingssyndrom
- 22q13.3 Slettingssyndrom
- 47 XXX syndrom
- 47, XYY-syndrom
- 5-nukleotidasesyndrom
- 5q- syndrom