orphafolder

| 264745 | Secondary interstitial lung disease specific to adulthood associated with a systemic disease
| 2934 | Polysyndactyly-cardiac malformation syndrome
| 264750 | Langerhans cell histiocytosis specific to adulthood
| 264757 | Interstitial lung disease in childhood and adulthood
| 264762 | Primary interstitial lung disease in childhood and adulthood
| 264930 | Primary interstitial lung disease in childhood and adulthood due to alveolar structure disorder
| 264935 | Primary interstitial lung disease in childhood and adulthood due to alveolar vascular disorder
| 2941 | Porencephaly-cerebellar hypoplasia-internal malformations syndrome
| 264944 | Secondary interstitial lung disease in childhood and adulthood
| 2940 | Porencephaly
| 2896 | Pitt-Hopkins syndrome
| 2899 | Brachyolmia-amelogenesis imperfecta syndrome
| 2900 | Leri pleonosteosis
| 264431 | Partial duplication of the short arm of chromosome 1
| 2905 | POEMS syndrome
| 264450 | Trisomy 8p
| 2907 | Hereditary acrokeratotic poikiloderma
| 2911 | Poland syndrome
| 264580 | Glycogen storage disease due to liver phosphorylase kinase deficiency
| 264656 | Interstitial lung disease specific to childhood
| 264670 | Primary interstitial lung disease specific to childhood due to alveolar structure disorder
| 2916 | Postaxial polydactyly-dental and vertebral anomalies syndrome
| 264665 | Primary interstitial lung disease specific to childhood
| 2917 | Polydactyly-myopia syndrome
| 264683 | Primary interstitial lung disease specific to childhood due to alveolar vascular disorder
| 2919 | Orofaciodigital syndrome type 5
| 264675 | Hereditary pulmonary alveolar proteinosis
| 2920 | Oliver syndrome
| 264691 | Isolated pulmonary capillaritis
| 2921 | Preaxial polydactyly-colobomata-intellectual disability syndrome
| 264688 | Congenital chylothorax
| 3374 | Triopia
| 275803 | Pulmonary arterial hypertension associated with congenital heart disease
| 275808 | Pulmonary arterial hypertension associated with HIV infection
| 275813 | Pulmonary arterial hypertension associated with portal hypertension
| 1717 | Distal trisomy 19q
| 3377 | Trismus-pseudocamptodactyly syndrome
| 275823 | Pulmonary arterial hypertension associated with schistosomiasis
| 3368 | Trigonocephaly-bifid nose-acral anomalies syndrome
| 275777 | Heritable pulmonary arterial hypertension
| 275786 | Drug- or toxin-induced pulmonary arterial hypertension
| 275791 | Pulmonary arterial hypertension associated with another disease
| 3369 | Trigonocephaly-short stature-developmental delay syndrome
| 275798 | Pulmonary arterial hypertension associated with connective tissue disease
| 3363 | Trichomegaly-retina pigmentary degeneration-dwarfism syndrome
| 275749 | Beta-thalassemia and related diseases
| 275752 | Sickle cell disease and related diseases
| 3366 | Isolated trigonocephaly
| 275761 | Lysosomal acid lipase deficiency
| 3365 | Trigonocephaly-broad thumbs syndrome
| 275766 | Idiopathic pulmonary arterial hypertension
| 275729 | Rare hemorrhagic disorder due to a constitutional thrombocytopenia
| 275736 | Rare hemorrhagic disorder due to a qualitative platelet defect
| 3361 | Trichodysplasia-xeroderma syndrome
| 275742 | Genetic infertility
| 275745 | Alpha-thalassemia and related diseases
| 3408 | Upington disease
| 276148 | Benign epithelial tumor of salivary glands
| 3409 | Urban-Rogers-Meyer syndrome
| 276145 | Malignant epithelial tumor of salivary glands
| 276161 | Multiple endocrine neoplasia
| 3412 | VACTERL with hydrocephalus
| 276152 | Multiple endocrine neoplasia type 4
| 3391 | Odonto-onycho-hypohidrotic dysplasia-midline scalp defects syndrome
| 276061 | Genetic frontotemporal degeneration with dementia
| 3403 | Uhl anomaly
| 276058 | Genetic neurodegenerative disease with dementia
| 3404 | Ulbright-Hodes syndrome
| 276142 | Rare tumor of salivary glands
| 276066 | Bile acid CoA ligase deficiency and defective amidation
| 275872 | Frontotemporal dementia with motor neuron disease
| 3383 | Humerus trochlea aplasia
| 3384 | Truncus arteriosus
| 275864 | Behavioral variant of frontotemporal dementia
| 275944 | Hemolytic disease of the newborn with Kell alloimmunization
| 3387 | Isolated anterior cervical hypertrichosis
| 3388 | Neural tube defect
| 275938 | Hemolytic disease due to fetomaternal alloimmunization
| 275837 | Pulmonary hypertension owing to lung disease and/or hypoxia
| 1723 | Mosaic trisomy 2
| 275828 | Pulmonary arterial hypertension associated with chronic hemolytic anemia
| 1724 | Mosaic trisomy 20
| 275853 | Syndrome with pulmonary hypertension as a major feature
| 1747 | Mosaic trisomy 7
| 275844 | Pulmonary hypertension with unclear multifactorial mechanism
| 271841 | Genetic cardiac tumor
| 3333 | Connective tissue dysplasia, Spellacy type
| 271832 | Genetic soft tissue tumor
| 271835 | Genetic digestive tract tumor
| 3332 | Hypoplastic tibiae-postaxial polydactyly syndrome
| 3329 | Tibial aplasia-ectrodactyly syndrome
| 3328 | Absent tibia-polydactyly-arachnoid cyst syndrome
| 3327 | Thyrocerebrorenal syndrome
| 3326 | Thymic-renal-anal-lung dysplasia
| 3323 | Thrombocytopenia-Robin sequence syndrome
| 3322 | Hoyeraal-Hreidarsson syndrome
| 3317 | Thoracolaryngopelvic dysplasia
| 3316 | Thomas syndrome
| 3314 | Thiemann disease, familial form
| 3355 | Trichoodontoonychial dysplasia

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