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Table 4: List of Rare Diseases and Related Terms as per US ...

Table 4: List of Rare Diseases and Related Terms as per US ...

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3009 Ichthyosis prematurity syndrome<br />

3010 Ichthyosis ta<strong>per</strong>ed fingers midline groove up<br />

3011 Ichthyosis vulgaris<br />

3012 Ichthyosis with hypotrichosis, autosomal recessive<br />

3013 Ichthyosis, acquired<br />

3014 Ichthyosis, erythrokeratolysis hemalis<br />

3015 Ichthyosis, follicular<br />

3016 Ichthyosis, leukocyte vacuoles, alopecia, <strong>and</strong> sclerosing<br />

cholangitis<br />

3017 Ichthyosis, mental retardation, dwarfism <strong>and</strong> renal impairment<br />

3018 Ichthyosis-mental retardation syndrome with large keratohyalin<br />

granules in the skin<br />

3019 Idiopathic acute eosinophilic pneumonia<br />

3020 Idiopathic adolescent scoliosis<br />

3021 Idiopathic alveolar hypoventilation syndrome<br />

3022 Idiopathic b<strong>as</strong>al ganglia calcification childhood-onset<br />

3023 Idiopathic diffuse interstitial fibrosis<br />

3024 Idiopathic dilatation <strong>of</strong> the pulmonary artery<br />

3025 Idiopathic double athetosis<br />

3026 Idiopathic eosinophilic chronic pneumopathy<br />

3027 Idiopathic juxtafoveal retinal telangiect<strong>as</strong>ia<br />

3028 Idiopathic myopathy<br />

3029 Idiopathic pulmonary fibrosis<br />

3030 Idiopathic pulmonary hemosiderosis<br />

3031 Idiopathic pulmonary hy<strong>per</strong>tension<br />

3032 Idiopathic spinal cord herniation<br />

3033 Idiopathic subglottic tracheal stenosis<br />

3034 Idiopathic thrombocytopenic purpura<br />

3035 Iida Kannari syndrome<br />

3036 IL12RB1 deficiency<br />

3037 Illum syndrome<br />

3038 Imaizumi Kuroki syndrome<br />

3039 Imerslund-Gr<strong>as</strong>beck syndrome<br />

3040 Iminoglycinuria<br />

3041 Immotile cilia syndrome, due to defective radial spokes<br />

3042 Immune defect due to absence <strong>of</strong> thymus<br />

3043 Immune deficiency, familial variable<br />

3044 Immune dysfunction with T-cell inactivation due to calcium entry<br />

defect 1

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