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| 615 | Familial atrial myxoma
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| 874 | Primary adult heart tumor
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| 1330 | Partial atrioventricular canal
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| 1677 | Familial idiopathic dilatation of the right atrium
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| 720 | Pili bifurcati
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| 671 | Primary cutis verticis gyrata
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| 864 | Trichofolliculoma
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| 247 | Arrhythmogenic right ventricular cardiomyopathy
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| 444 | Marie Unna hereditary hypotrichosis
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| 2221 | Acquired hypertrichosis lanuginosa
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| 492 | Proliferating trichilemmal cyst
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| 499 | Kerion celsi
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| 573 | Monilethrix
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| 525 | Lichen planopilaris
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| 700 | Alopecia totalis
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| 840 | Syringocystadenoma papilliferum
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| 384 | Huriez syndrome
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| 315 | Erythrokeratoderma ''en cocardes''
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| 338 | Familial multiple fibrofolliculoma
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| 409 | Hyperkeratosis lenticularis perstans
-
| 496 | Thost-Unna palmoplantar keratoderma
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| 41 | Dyschromatosis symmetrica hereditaria
-
| 122 | Birt-Hogg-Dubé syndrome
-
| 38 | Acrokeratoelastoidosis of Costa
-
| 39 | Acromelanosis
-
| 241 | Dyschromatosis universalis hereditaria
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| 316 | Progressive symmetric erythrokeratodermia
-
| 211 | Familial cylindromatosis
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| 435 | Ito hypomelanosis
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| 658 | Non-histaminic angioedema
-
| 3282 | Multifocal atrial tachycardia
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| 188 | Systemic capillary leak syndrome
-
| 303 | Dystrophic epidermolysis bullosa
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| 305 | Junctional epidermolysis bullosa
-
| 3406 | Ulerythema ophryogenesis
-
| 2908 | Kindler syndrome
-
| 81 | Antisynthetase syndrome
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| 563 | Peripartum cardiomyopathy
-
| 764 | Pyomyositis
-
| 779 | Reynolds syndrome
-
| 838 | Susac syndrome
-
| 889 | Cutaneous small vessel vasculitis
-
| 482 | Kimura disease
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| 31828 | Digitalis poisoning
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| 31837 | Pulmonary venoocclusive disease
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| 31740 | Hypersensitivity pneumonitis
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| 31709 | Infantile convulsions and choreoathetosis
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| 31826 | Ethylene glycol poisoning
-
| 31827 | Paraquat poisoning
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| 31824 | Colchicine poisoning
-
| 31825 | Methanol poisoning
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| 31205 | Rat-bite fever
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| 31204 | Nocardiosis
-
| 31154 | Hypobetalipoproteinemia
-
| 31202 | Melioidosis
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| 31150 | Tangier disease
-
| 31153 | Hypoalphalipoproteinemia
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| 31142 | Oral erosive lichen
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| 31043 | Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement
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| 31112 | Dermatofibrosarcoma protuberans
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| 30924 | Primary hypomagnesemia with secondary hypocalcemia
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| 30925 | Hereditary central diabetes insipidus
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| 71278 | Congenital brain dysgenesis due to glutamine synthetase deficiency
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| 71279 | CANOMAD syndrome
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| 71281 | Rare central nervous system and retinal vascular disease
-
| 71271 | Split hand-split foot-deafness syndrome
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| 71272 | Sandifer syndrome
-
| 71273 | Renal nutcracker syndrome
-
| 71274 | Disseminated peritoneal leiomyomatosis
-
| 71275 | Rh deficiency syndrome
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| 71276 | Silent sinus syndrome
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| 71277 | Encephalopathy due to GLUT1 deficiency
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| 71209 | Rare soft tissue tumor
-
| 71212 | Hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency
-
| 71211 | Neuromyelitis optica
-
| 71267 | Dentinogenesis imperfecta-short stature-hearing loss-intellectual disability syndrome
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| 71213 | Retinal capillary malformation
-
| 71198 | Rare pulmonary hypertension
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| 71203 | Autoimmune thrombocytopenia
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| 71202 | Rare hemorrhagic disorder due to a constitutional platelet anomaly
-
| 70591 | Chronic thromboembolic pulmonary hypertension
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| 70592 | Immunodeficiency due to interleukin-1 receptor-associated kinase-4 deficiency
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| 70589 | Bronchopulmonary dysplasia
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| 70590 | Infantile apnea
-
| 70595 | Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome
-
| 70596 | Congenital Epstein-Barr virus infection
-
| 70593 | Immunodeficiency due to selective anti-polysaccharide antibody deficiency
-
| 70594 | Dopa-responsive dystonia due to sepiapterin reductase deficiency
-
| 70578 | Adult acute respiratory distress syndrome
-
| 70573 | Small cell lung cancer
-
| 70568 | Post-transplant lymphoproliferative disease
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| 70588 | Meconium aspiration syndrome
-
| 70587 | Infant acute respiratory distress syndrome
-
| 70474 | Leigh syndrome with cardiomyopathy
-
| 70472 | Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type
-
| 70470 | Hyperlipoproteinemia type 5
-
| 70567 | Cholangiocarcinoma
-
| 70482 | Carcinoma of esophagus
-
| 70476 | Vernal keratoconjunctivitis
-
| 70475 | Radiation proctitis
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