Wyszukiwarka

Serwis Ministerstwa Zdrowia i Narodowego Funduszu Zdrowia

Lista chorób rzadkich*

Wyszukiwarka
2822 - Autosomal recessive spastic paraplegia type 11
2823 - OBSOLETE: Paraplegia-brachydactyly-cone-shaped epiphysis syndrome
2824 - Paraplegia-intellectual disability-hyperkeratosis syndrome
2825 - PARC syndrome
2826 - Spastic paraplegia-precocious puberty syndrome
2828 - Young-onset Parkinson disease
2829 - Partington-Anderson syndrome
2831 - Rhizomelic dysplasia, Patterson-Lowry type
2832 - Short tarsus-absence of lower eyelashes syndrome
2833 - Stiff skin syndrome
2834 - Wrinkly skin syndrome
2835 - Pectus excavatum-macrocephaly-dysplastic nails syndrome
2836 - PEHO syndrome
2837 - Pellagra-like skin rash-neurological manifestations syndrome
2838 - Renal caliceal diverticuli-deafness syndrome
2839 - Pelvis-shoulder dysplasia
2840 - Pelvic dysplasia-arthrogryposis of lower limbs syndrome
2841 - Familial benign chronic pemphigus
2842 - Penoscrotal transposition
2843 - Pentosuria
2846 - Congenital pericardium anomaly
2847 - Pericardial and diaphragmatic defect
2848 - Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome
2849 - Perlman syndrome
2850 - Alopecia-intellectual disability syndrome
2853 - Serpentine fibula-polycystic kidneys syndrome
2854 - Fuhrmann syndrome
2855 - Perrault syndrome
2856 - Persistent Müllerian duct syndrome
2860 - OBSOLETE: Preeyasombat-Varavithya syndrome
2861 - OBSOLETE: Short stature-microcephaly-heart defect syndrome
2863 - Short stature-wormian bones-dextrocardia syndrome
2864 - OBSOLETE: Short stature-prognathism-short femoral necks syndrome
2865 - Short stature-webbed neck-heart disease syndrome
2866 - Short stature-deafness-neutrophil dysfunction-dysmorphism syndrome
2867 - Short stature, Brussels type
2868 - Short stature-valvular heart disease-characteristic facies syndrome
2869 - Peutz-Jeghers syndrome
2870 - NON RARE IN EUROPE: Peyronie syndrome
2871 - Pfeiffer-Palm-Teller syndrome
2872 - Cardiocranial syndrome, Pfeiffer type
2874 - Phakomatosis pigmentokeratotica
2875 - Phakomatosis pigmentovascularis
2876 - PHAVER syndrome
2878 - Phocomelia-ectrodactyly-deafness-sinus arrhythmia syndrome
2879 - Phocomelia, Schinzel type
2880 - Phosphoenolpyruvate carboxykinase deficiency
2881 - Cutaneous photosensitivity-lethal colitis syndrome
2882 - Sitosterolemia
2884 - Piebaldism
*Źródło

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