Wyszukiwarka

Serwis Ministerstwa Zdrowia i Narodowego Funduszu Zdrowia

Lista chorób rzadkich*

Wyszukiwarka
98681 - Rare disorder with strabismus
98682 - NON RARE IN EUROPE: Essential strabismus
98683 - Syndromic disorder with strabismus
98684 - Craniostenosis with strabismus
98685 - Rare oculomotor nerve disorder
98686 - Congenital trochlear nerve palsy
98687 - Supranuclear eye movement disorder
98688 - Oculomotor apraxia
98689 - OBSOLETE: Myopathy with eye involvement
98690 - OBSOLETE: Myasthenic syndrome with eye involvement
98691 - OBSOLETE: Abnormal eye movements
98692 - OBSOLETE: Nervous system anomaly with eye involvement
98693 - OBSOLETE: Spinocerebellar ataxia with oculomotor anomaly
98694 - OBSOLETE: Spinocerebellar degenerescence and spastic paraparesis with an oculomotor anomaly
98695 - OBSOLETE: Mitochondrial disease with eye involvement
98696 - OBSOLETE: Genodermatosis with ocular features
98697 - OBSOLETE: Genetic keratinization disorder associated with ocular features
98698 - OBSOLETE: Ichthyosis associated with ocular features
98699 - OBSOLETE: Syndromic ichthyosis associated with ocular features
98700 - OBSOLETE: Pigmentation disorder with eye involvement
98701 - OBSOLETE: Phakomatosis with eye involvement
98702 - OBSOLETE: Connective tissue disease with eye involvement
98703 - OBSOLETE: Disease with potential neoplastic degeneration associated with ocular features
98704 - OBSOLETE: Onycho-patellar syndrome with eye involvement
98706 - Oculocutaneous or ocular albinism
98708 - OBSOLETE: Pigmentation disorder with eye involvement, excluding albinism
98709 - OBSOLETE: Ectodermal malformation syndrome associated with ocular features
98710 - OBSOLETE: Metabolic disease associated with ocular features
98711 - OBSOLETE: Metabolic disease with corneal opacity
98712 - OBSOLETE: Metabolic disease with cataract
98713 - OBSOLETE: Metabolic disease with pigmentary retinitis
98714 - OBSOLETE: Metabolic disease with macular cherry-red spot
98715 - Uveitis
98716 - Heart position anomaly
98717 - Transposition of the great arteries and conotruncal cardiac anomaly
98718 - Aortic malformation
98719 - Pulmonary artery or pulmonary branch anomaly
98720 - Atrioventricular valve anomaly
98721 - Congenital tricuspid malformation
98722 - Atrioventricular septal defect
98723 - Hypoplastic right heart syndrome
98724 - Congenital anomaly of the great arteries
98725 - Ascending aorta anomaly
98726 - OBSOLETE: Pulmonary artery/pulmonary branch anomaly
98727 - Rare atrial defect and interatrial communication
98729 - Congenital pulmonary veins anomaly
98730 - OBSOLETE: Atrioventricular discordance
98731 - Congenital arteriovenous fistula
98732 - OBSOLETE: Syndrome associated with a congenital cardiopathy
98733 - Noonan syndrome and Noonan-related syndrome
*Źródło

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