Wyszukiwarka

Serwis Ministerstwa Zdrowia i Narodowego Funduszu Zdrowia

Lista chorób rzadkich*

Wyszukiwarka
157719 - Juvenile or adult CACH syndrome
157769 - Situs ambiguus
157788 - Hypospadias-hypertelorism-coloboma and deafness syndrome
157791 - Epithelioid hemangioendothelioma
157794 - Hereditary mixed polyposis syndrome
157798 - Serrated polyposis syndrome
157801 - Mesoaxial synostotic syndactyly with phalangeal reduction
157808 - Congenital pseudoarthrosis of the limbs
157820 - Cold-induced sweating syndrome
157823 - Klüver-Bucy syndrome
157826 - Congenital epulis
157832 - Craniorhiny
157835 - Paroxysmal hemicrania
157843 - Trigeminal autonomic cephalalgia
157846 - Neuroferritinopathy
157850 - Pantothenate kinase-associated neurodegeneration
157855 - HARP syndrome
157941 - Huntington disease-like 1
157946 - Huntington disease-like 3
157949 - Combined immunodeficiency with granulomatosis
157954 - ANE syndrome
157962 - Oculoauricular syndrome, Schorderet type
157965 - SLC39A13-related spondylodysplastic Ehlers-Danlos syndrome
157973 - Congenital muscular dystrophy due to LMNA mutation
157980 - NON RARE IN EUROPE: Bladder cancer
157987 - Non-Langerhans cell histiocytosis
157991 - Generalized eruptive histiocytosis
157997 - Benign cephalic histiocytosis
158000 - Juvenile xanthogranuloma
158003 - Xanthoma disseminatum
158008 - Papular xanthoma
158011 - Necrobiotic xanthogranuloma
158014 - Rosaï-Dorfman disease
158019 - Indeterminate cell histiocytosis
158022 - Progressive nodular histiocytosis
158025 - Hereditary progressive mucinous histiocytosis
158029 - Sea-blue histiocytosis
158032 - Hemophagocytic syndrome
158038 - Primary hemophagocytic lymphohistiocytosis
158041 - Secondary hemophagocytic lymphohistiocytosis
158048 - Hemophagocytic syndrome associated with an infection
158057 - Acquired hemophagocytic lymphohistiocytosis associated with malignant disease
158061 - Macrophage activation syndrome
158124 - Genetic dementia
158266 - Huntington disease-like syndrome
158300 - Rare genetic hematologic disease
158661 - OBSOLETE: Suprabasal epidermolysis bullosa simplex
158665 - OBSOLETE: Basal epidermolysis bullosa simplex
158668 - Ectodermal dysplasia-skin fragility syndrome
158673 - Localized dystrophic epidermolysis bullosa, acral form
*Źródło

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

  • Logotyp - Ministerstwo Zdrowia
  • Logotyp - Centrum e-Zdrowia

© 2023 Centrum e-Zdrowia. Wszystkie prawa zastrzeżone