Wyszukiwarka

Serwis Ministerstwa Zdrowia i Narodowego Funduszu Zdrowia

Lista chorób rzadkich*

Wyszukiwarka
99771 - Bifid uvula
99772 - Cleft velum
99776 - Mosaic trisomy 9
99777 - Achalasia-alacrimia syndrome
99781 - OBSOLETE: Familial articular chondrocalcinosis type 1
99782 - OBSOLETE: Familial articular chondrocalcinosis type 2
99789 - Dentin dysplasia type I
99791 - Dentin dysplasia type II
99792 - Dentin dysplasia-sclerotic bones syndrome
99796 - Subcortical band heterotopia
99797 - Anodontia
99798 - Oligodontia
99802 - Hemimegalencephaly
99803 - Haddad syndrome
99806 - Oculootodental syndrome
99807 - PEHO-like syndrome
99810 - Familial porencephaly
99811 - Neuronal intestinal pseudoobstruction
99812 - LIG4 syndrome
99817 - Non-polyposis Turcot syndrome
99818 - Turcot syndrome with polyposis
99819 - Familial gestational hyperthyroidism
99824 - Lassa fever
99825 - Nipah virus disease
99826 - Marburg hemorrhagic fever
99827 - Crimean-Congo hemorrhagic fever
99828 - Dengue fever
99829 - Yellow fever
99831 - OBSOLETE: Common variable immunodeficiency due to an intrinsic T cell defect
99832 - Resistance to thyrotropin-releasing hormone syndrome
99842 - Leukocyte adhesion deficiency type I
99843 - Leukocyte adhesion deficiency type II
99844 - Leukocyte adhesion deficiency type III
99845 - Genetic recurrent myoglobinuria
99846 - Autosomal dominant myoglobinuria
99849 - Glycogen storage disease due to muscle beta-enolase deficiency
99852 - Ravine syndrome
99853 - Ovarioleukodystrophy
99854 - Cree leukoencephalopathy
99856 - Primary syringomyelia
99857 - Secondary syringomyelia
99858 - Idiopathic syringomyelia
99859 - OBSOLETE: Posttraumatic syringomyelia
99860 - Precursor B-cell acute lymphoblastic leukemia
99861 - Precursor T-cell acute lymphoblastic leukemia
99864 - OBSOLETE: Classic seminoma
99865 - Spermatocytic seminoma
99866 - OBSOLETE: Metastatic spermatocytic seminoma
99867 - Thymoma
99868 - Thymic carcinoma
*Źródło

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