Lista chorób rzadkich*

55654 - Hypotrichosis simplex

55655 - Pneumococcal meningitis

55880 - Chondrosarcoma

55881 - Adamantinoma

56044 - Carcinoma of gallbladder and extrahepatic biliary tract

56304 - Atelosteogenesis type II

56305 - Atelosteogenesis type III

56425 - Cold agglutinin disease

56965 - Progressive bulbar paralysis of childhood

56970 - Human prion disease

57145 - SUNCT syndrome

57146 - Rare hepatic disease

57194 - OBSOLETE: Aseptic osteitis

57196 - Medial condensing osteitis of the clavicle

57777 - Cirrhotic cardiomyopathy

57782 - Mazabraud syndrome

58017 - Classic hairy cell leukemia

58040 - Osteoblastoma

58208 - NON RARE IN EUROPE: Pericarditis

58220 - OBSOLETE: Microscopic colitis

59135 - Laing early-onset distal myopathy

59181 - Sorsby pseudoinflammatory fundus dystrophy

59298 - Schilder disease

59303 - Neonatal ichthyosis-sclerosing cholangitis syndrome

59305 - Gestational trophoblastic neoplasm

59306 - McLeod neuroacanthocytosis syndrome

59315 - Rhombencephalosynapsis

60014 - Argyria

60015 - Enlarged parietal foramina

60025 - Pulmonary alveolar microlithiasis

60026 - Pulmonary nodular lymphoid hyperplasia

60030 - Loeys-Dietz syndrome

60032 - Recurrent respiratory papillomatosis

60033 - Idiopathic bronchiectasis

60039 - Pudendal neuralgia

60040 - Megalencephaly-capillary malformation-polymicrogyria syndrome

60041 - Congenital heart block

63259 - Iniencephaly

63260 - Craniorachischisis

63261 - HERNS syndrome

63269 - Antley-Bixler syndrome with genital anomaly and disorder of steroidogenesis

63273 - Distal myopathy with posterior leg and anterior hand involvement

63275 - Pemphigoid gestationis

63440 - OBSOLETE: Isolated oxycephaly

63442 - Angel-shaped phalango-epiphyseal dysplasia

63443 - Rare epithelial tumor of stomach

63446 - Acrocapitofemoral dysplasia

63454 - Pattern dystrophy

63455 - Paraneoplastic pemphigus

63862 - Schisis association

Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl

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