Wyszukiwarka

Serwis Ministerstwa Zdrowia i Narodowego Funduszu Zdrowia

Lista chorób rzadkich*

Wyszukiwarka
63999 - IgG4-related mediastinitis
64280 - Childhood absence epilepsy
64542 - Acrofacial dysostosis, Kennedy-Teebi type
64545 - Benign idiopathic neonatal seizures
64686 - Tolosa-Hunt syndrome
64692 - Oroya fever
64694 - Trench fever
64720 - Leiomyosarcoma
64722 - Granulomatous mastitis
64734 - Iridocorneal endothelial syndrome
64738 - NON RARE IN EUROPE: Non rare thrombophilia
64739 - Ovarian hyperstimulation syndrome
64740 - NON RARE IN EUROPE: Recurrent acute pancreatitis
64741 - Pulmonary blastoma
64742 - Pleuropulmonary blastoma
64743 - Hepatoportal sclerosis
64744 - IgG4-related thyroid disease
64745 - Pruritic urticarial papules and plaques of pregnancy
64746 - Autosomal dominant Charcot-Marie-Tooth disease type 2
64747 - X-linked Charcot-Marie-Tooth disease
64748 - Dejerine-Sottas syndrome
64749 - Charcot-Marie-Tooth disease type 4
64751 - Hereditary motor and sensory neuropathy type 5
64752 - Hereditary sensory and autonomic neuropathy type 5
64753 - Spinocerebellar ataxia with axonal neuropathy type 2
64754 - Nevus comedonicus syndrome
64755 - Becker nevus syndrome
65250 - Perineural cyst
65279 - OBSOLETE: Lymphocytic colitis
65282 - Carvajal syndrome
65283 - Timothy syndrome
65284 - Biotin-thiamine-responsive basal ganglia disease
65285 - Lhermitte-Duclos disease
65286 - 3q29 microdeletion syndrome
65287 - Beta-ureidopropionase deficiency
65288 - Permanent neonatal diabetes mellitus-pancreatic and cerebellar agenesis syndrome
65681 - Vaginal atresia
65682 - Benign recurrent intrahepatic cholestasis
65683 - Isolated focal cortical dysplasia
65684 - Monomelic amyotrophy
65720 - Arthrogryposis-severe scoliosis syndrome
65743 - Autosomal dominant multiple pterygium syndrome
65748 - Multiple self-healing squamous epithelioma
65753 - Charcot-Marie-Tooth disease type 1
65759 - Carpenter syndrome
65798 - Goodman syndrome
66518 - Short fifth metacarpals-insulin resistance syndrome
66529 - Tako-Tsubo cardiomyopathy
66624 - PANDAS
66625 - Cerebrooculonasal syndrome
*Źródło

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