Wyszukiwarka

Serwis Ministerstwa Zdrowia i Narodowego Funduszu Zdrowia

Lista chorób rzadkich*

Wyszukiwarka
163903 - OBSOLETE: Limbic encephalitis associated with antibodies to cell membrane antigens
163908 - OBSOLETE: Limbic encephalitis with LGI1 antibodies
163914 - OBSOLETE: Limbic encephalitis with nCMAgs antibodies
163918 - OBSOLETE: Non-paraneoplastic limbic encephalitis
163921 - Posttransplant acute limbic encephalitis
163924 - OBSOLETE: Non-herpetic acute limbic encephalitis
163927 - Pustulosis palmaris et plantaris
163931 - Acrodermatitis continua of Hallopeau
163934 - Atopic keratoconjunctivitis
163937 - X-linked intellectual disability, Najm type
163953 - X-linked intellectual disability, Raymond type
163956 - X-linked intellectual disability, Nascimento type
163961 - X-linked cerebral-cerebellar-coloboma syndrome
163966 - X-linked dominant chondrodysplasia, Chassaing-Lacombe type
163971 - X-linked intellectual disability, Cilliers type
163976 - X-linked intellectual disability, Van Esch type
163979 - X-linked intellectual disability-craniofacioskeletal syndrome
163982 - X-linked intellectual disability-spastic quadriparesis syndrome
163985 - Hyperekplexia-epilepsy syndrome
163988 - OBSOLETE: Developmental delay-deafness syndrome, Hildebrand type
164001 - Rare odontal or periodontal disorder
164004 - Middle and/or inner ear anomaly
164726 - Acute myeloid leukemia and myelodysplastic syndromes related to radiation
164736 - Familial advanced sleep-phase syndrome
164823 - Rare acquired aplastic anemia
165652 - Rare genetic gastroenterological disease
165655 - Genetic intestinal disease
165658 - Genetic gastro-esophageal disease
165661 - Genetic pancreatic disease
165704 - Non-syndromic urogenital tract malformation
165707 - Syndromic urogenital tract malformation
165711 - Rare abdominal surgical disease
165805 - Familial mesial temporal lobe epilepsy with febrile seizures
165955 - Wound myiasis
165958 - Cavitary myiasis
165961 - OBSOLETE: Subcutaneous myiasis
165985 - Diazoxide-sensitive diffuse hyperinsulinism
165988 - Diazoxide-resistant diffuse hyperinsulinism
165991 - Exercise-induced hyperinsulinism
165994 - Pituitary resistance to thyroid hormone
166002 - Multiple epiphyseal dysplasia due to collagen 9 anomaly
166011 - Multiple epiphyseal dysplasia, Beighton type
166016 - Multiple epiphyseal dysplasia, Lowry type
166024 - Multiple epiphyseal dysplasia, Al-Gazali type
166029 - Multiple epiphyseal dysplasia, with severe proximal femoral dysplasia
166032 - Multiple epiphyseal dysplasia, with miniepiphyses
166035 - Brachydactyly-short stature-retinitis pigmentosa syndrome
166038 - Metaphyseal chondrodysplasia, Kaitila type
166063 - Pontocerebellar hypoplasia type 4
166068 - Pontocerebellar hypoplasia type 5
*Źródło

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