-
| 272 | Congenital muscular dystrophy, Fukuyama type
-
| 265 | Autosomal dominant limb-girdle muscular dystrophy type 1C
-
| 268 | Autosomal recessive limb-girdle muscular dystrophy type 2B
-
| 263 | Limb-girdle muscular dystrophy
-
| 600 | Vocal cord and pharyngeal distal myopathy
-
| 609 | Tibial muscular dystrophy
-
| 602 | GNE myopathy
-
| 68 | Amoebiasis due to free-living amoebae
-
| 781 | Q fever
-
| 302 | Epidermodysplasia verruciformis
-
| 297 | Tick-borne encephalitis
-
| 182 | Chromomycosis
-
| 128 | Diphyllobothriasis
-
| 283 | Demodicidosis
-
| 210 | Cyclosporosis
-
| 76 | Strongyloidiasis
-
| 74 | Angiostrongyliasis
-
| 108 | Babesiosis
-
| 78 | Ankylostomiasis
-
| 129 | Pseudopelade of Brocq
-
| 123 | Björnstad syndrome
-
| 898 | Wagner disease
-
| 518 | Acute megakaryoblastic leukemia
-
| 318 | Acute erythroid leukemia
-
| 514 | Acute monoblastic leukemia
-
| 517 | Acute myelomonocytic leukemia
-
| 505 | Graham Little-Piccardi-Lassueur syndrome
-
| 346 | Quinquaud's folliculitis decalvans
-
| 222 | Erosive pustular dermatosis of the scalp
-
| 202 | Crandall syndrome
-
| 170 | Woolly hair
-
| 169 | Ringed hair disease
-
| 168 | Loose anagen syndrome
-
| 345 | Dissecting cellulitis of the scalp
-
| 591 | Furuncular myiasis
-
| 723 | Pneumocystosis
-
| 472 | Isosporiasis
-
| 504 | Creeping myiasis
-
| 401 | Hymenolepiasis
-
| 390 | Histoplasmosis
-
| 400 | Cystic echinococcosis
-
| 520 | Acute promyelocytic leukemia
-
| 450 | Heterotaxia
-
| 529 | Roch-Leri mesosomatous lipomatosis
-
| 224 | Neonatal diabetes mellitus
-
| 826 | Sporotrichosis
-
| 879 | Tungiasis
-
| 432 | Normosmic congenital hypogonadotropic hypogonadism
-
| 91 | Aromatase deficiency
-
| 785 | Estrogen resistance syndrome
-
| 873 | Desmoid tumor
-
| 553 | Cushing syndrome
-
| 679 | Malignant atrophic papulosis
-
| 901 | Wells syndrome
-
| 703 | Bullous pemphigoid
-
| 841 | Sebocystomatosis
-
| 817 | Peeling skin syndrome
-
| 867 | Familial multiple trichoepithelioma
-
| 735 | Porokeratosis of Mibelli
-
| 659 | Mutilating palmoplantar keratoderma with periorificial keratotic plaques
-
| 737 | Porokeratosis plantaris palmaris et disseminata
-
| 736 | Palmoplantar porokeratosis of Mantoux
-
| 523 | Hereditary leiomyomatosis and renal cell cancer
-
| 314 | Erythroderma desquamativum
-
| 623 | NAME syndrome
-
| 530 | Lipoid proteinosis
-
| 493 | Familial keratoacanthoma
-
| 498 | Keratosis pilaris atrophicans
-
| 454 | Acquired ichthyosis
-
| 490 | Omphalomesenteric cyst
-
| 238 | Digestive duplication
-
| 617 | Congenital primary megaureter
-
| 488 | Urachal cyst
-
| 105 | Atresia of urethra
-
| 237 | Duplication of urethra
-
| 734 | Alpha delta granule deficiency
-
| 721 | Gray platelet syndrome
-
| 722 | Hypoplasminogenemia
-
| 749 | Congenital prekallikrein deficiency
-
| 853 | Fetal and neonatal alloimmune thrombocytopenia
-
| 483 | Congenital high-molecular-weight kininogen deficiency
-
| 852 | X-linked thrombocytopenia with normal platelets
-
| 465 | Congenital plasminogen activator inhibitor type 1 deficiency
-
| 310 | Reflex epilepsy
-
| 1332 | Medullary thyroid carcinoma
-
| 877 | Neuroendocrine neoplasm
-
| 73 | Gorham-Stout disease
-
| 728 | Relapsing polychondritis
-
| 467 | Non-acquired combined pituitary hormone deficiency
-
| 142 | Anaplastic thyroid carcinoma
-
| 143 | Parathyroid carcinoma
-
| 759 | Central precocious puberty
-
| 786 | Glucocorticoid resistance
-
| 1676 | Idiopathic pulmonary artery dilatation
-
| 1666 | Dextrocardia
-
| 1461 | Criss-cross heart
-
| 1205 | Mitral atresia
-
| 3192 | Supravalvular pulmonary stenosis
-
| 875 | Primary pediatric heart tumor
-
| 334 | Familial atrial fibrillation
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