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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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505 Atrophoderma <strong>of</strong> Pierini <strong>and</strong> P<strong>as</strong>ini<br />

506 Atrophodermia vermiculata<br />

507 Attenuated familial adenomatous polyposis<br />

508 Atypical hemolytic uremic syndrome<br />

509 Atypical lipodystrophy<br />

510 Atypical mycobacteriosis, familial<br />

511 Atypical Rett syndrome<br />

512 Auditory neuropathy<br />

513 Auditory <strong>per</strong>ceptual disorder<br />

514 Auralcephalosyndactyly<br />

515 Auriculo-condylar syndrome<br />

516 Auriculoosteodyspl<strong>as</strong>ia<br />

517 Ausems Wittebol-Post Hennekam syndrome<br />

518 Autism with port-wine stain<br />

519 Autoimmune enteropathy<br />

520 Autoimmune hemolytic anemia<br />

521 Autoimmune hepatitis<br />

522 Autoimmune Inner Ear dise<strong>as</strong>e<br />

523 Autoimmune lymphoproliferative syndrome<br />

524 Autoimmune myocarditis<br />

525 Autoimmune oophoritis<br />

526 Autoimmune pancreatitis<br />

527 Autoimmune polygl<strong>and</strong>ular syndrome type 1<br />

528 Autoimmune polygl<strong>and</strong>ular syndrome type 2<br />

529 Autoimmune polygl<strong>and</strong>ular syndrome type 3<br />

530 Autoimmune progesterone dermatitis<br />

531 Autosomal dominant Alport syndrome<br />

532 Autosomal dominant compelling helio ophthalmic outburst<br />

syndrome<br />

533 Autosomal dominant hy<strong>per</strong> IgE syndrome<br />

534 Autosomal dominant neuronal ceroid lip<strong>of</strong>uscinosis 4B<br />

535 Autosomal dominant optic atrophy, hearing loss, <strong>and</strong> <strong>per</strong>ipheral<br />

neuropathy<br />

536 Autosomal dominant partial epilepsy with auditory features<br />

537 Autosomal dominant pseudohypoaldosteronism type 1<br />

538 Autosomal recessive Alport syndrome<br />

539 Autosomal recessive cerebellar ataxia with cabc1/adck3 gene<br />

mutations<br />

540 Autosomal recessive hy<strong>per</strong> IgE syndrome<br />

541 Autosomal recessive juvenile Parkinson dise<strong>as</strong>e

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