21:
217:
184:
33:
Generally, diseases outlined within the ICD-10 codes Q00-Q99 within
Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities should be included in this category.
789:
234:
385:
228:
660:
546:
375:
417:
412:
780:
729:
511:
402:
370:
608:
531:
266:
775:
541:
506:
491:
437:
638:
442:
359:
613:
551:
536:
476:
348:
486:
804:
719:
714:
427:
343:
261:
763:
734:
256:
692:
353:
814:
166:
163:
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157:
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118:
115:
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109:
106:
103:
100:
97:
94:
91:
86:
471:
293:
283:
246:
687:
603:
28:
International
Statistical Classification of Diseases and Related Health Problems, 10th Revision
588:
578:
397:
566:
8:
819:
677:
623:
618:
496:
365:
202:
46:
665:
432:
318:
298:
809:
633:
628:
556:
313:
308:
278:
751:
593:
447:
407:
380:
323:
251:
72:
206:
724:
481:
460:
422:
41:
739:
697:
682:
598:
526:
521:
501:
333:
288:
798:
702:
655:
466:
227:
The following 93 pages are in this category, out of approximately 241 total.
62:
561:
338:
303:
650:
516:
81:
66:
328:
583:
54:
27:
181:
This category has the following subcategory, out of 18 total.
199:
386:
Pterin-4 alpha-carbinolamine dehydratase deficiency
796:
661:Umbilical cord ulceration and intestinal atresia
547:Spondyloepimetaphyseal dysplasia, Strudwick type
74:
376:Progressive familial intrahepatic cholestasis
26:This category reflects the organization of
418:Riboflavin-responsive exercise intolerance
229:This list may not reflect recent changes
224:Pages in category "Congenital disorders"
797:
403:Renal dysplasia-limb defects syndrome
371:Progressive cardiac conduction defect
609:Transient myeloproliferative disease
176:
15:
267:Ostravik-Lindemann-Solberg syndrome
13:
413:Renal–hepatic–pancreatic dysplasia
238:
188:
175:
14:
831:
730:Weissenbacher–Zweymüller syndrome
781:Zamzam–Sheriff–Phillips syndrome
542:Spondyloepimetaphyseal dysplasia
492:Sepiapterin reductase deficiency
19:
639:Tyrosine hydroxylase deficiency
512:Simpson–Golabi–Behmel syndrome
1:
360:Primary congenital lymphedema
614:Transposition (birth defect)
552:Spondyloperipheral dysplasia
532:Smith–Fineman–Myers syndrome
507:Shprintzen–Goldberg syndrome
438:Rosselli–Gulienetti syndrome
222:
7:
715:Waardenburg syndrome type 1
428:Ring chromosome 14 syndrome
262:Osteochondroprogenitor cell
10:
836:
776:Zadik–Barak–Levin syndrome
257:Orofaciodigital syndrome 1
40:The main article for this
39:
693:Velopharyngeal inadequacy
443:Rubinstein–Taybi syndrome
537:Snyder–Robinson syndrome
477:Saethre–Chotzen syndrome
349:Potocki–Shaffer syndrome
720:Walker–Warburg syndrome
472:Sacrococcygeal teratoma
344:Potocki–Lupski syndrome
294:Parastremmatic dwarfism
284:Papillary fibroelastoma
247:Oculoauricular syndrome
764:Young–Simpson syndrome
735:Wilson–Turner syndrome
688:Van der Woude syndrome
604:Toxocara malayasiensis
589:Tetra-amelia syndrome
487:Senior–Løken syndrome
398:Radioulnar synostosis
354:Prader–Willi syndrome
567:Structural variation
678:VACTERL association
624:Triphalangeal thumb
619:Trichothiodystrophy
497:Sequence (medicine)
366:Proboscis (anomaly)
65:that is present at
59:congenital disorder
47:Congenital disorder
805:Disability by type
666:Urofacial syndrome
433:Ring chromosome 15
319:Phosphate diabetes
299:Patterson syndrome
634:Triploid syndrome
629:Triple-A syndrome
579:Tay–Sachs disease
557:Status marmoratus
314:Pfeiffer syndrome
309:Persistent cloaca
279:Palatal obturator
38:
37:
827:
752:XX male syndrome
594:Thumb hypoplasia
463:
448:Rudiger syndrome
408:Renal hypoplasia
381:Proteus syndrome
362:
324:Pilotto syndrome
252:Opsismodysplasia
208:
201:
23:
22:
16:
835:
834:
830:
829:
828:
826:
825:
824:
815:Animal diseases
795:
794:
793:
787:
786:
785:
768:
756:
744:
725:Weaver syndrome
707:
670:
643:
571:
482:Seckel syndrome
461:Sacral agenesis
459:
452:
423:RIDDLE syndrome
390:
358:
271:
221:
215:
214:
213:
210:
209:
198:
174:
173:
172:
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77:
51:
31:
20:
12:
11:
5:
833:
823:
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817:
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792:) (next page)
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783:
778:
772:
769:
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760:
757:
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754:
748:
745:
743:
742:
740:Worth syndrome
737:
732:
727:
722:
717:
711:
708:
706:
705:
700:
698:Vestigial twin
695:
690:
685:
683:Vaginal septum
680:
674:
671:
669:
668:
663:
658:
653:
647:
644:
642:
641:
636:
631:
626:
621:
616:
611:
606:
601:
599:TORCH syndrome
596:
591:
586:
581:
575:
572:
570:
569:
564:
559:
554:
549:
544:
539:
534:
529:
527:Situs inversus
524:
522:Situs ambiguus
519:
514:
509:
504:
502:SHORT syndrome
499:
494:
489:
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479:
474:
469:
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394:
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368:
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346:
341:
336:
334:Ponseti method
331:
326:
321:
316:
311:
306:
301:
296:
291:
289:Parasitic twin
286:
281:
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259:
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220:) (next page)
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36:
35:
24:
9:
6:
4:
3:
2:
832:
821:
818:
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808:
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791:
790:previous page
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738:
736:
733:
731:
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723:
721:
718:
716:
713:
712:
709:
704:
703:Vici syndrome
701:
699:
696:
694:
691:
689:
686:
684:
681:
679:
676:
675:
672:
667:
664:
662:
659:
657:
656:Ulnar dimelia
654:
652:
649:
648:
645:
640:
637:
635:
632:
630:
627:
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622:
620:
617:
615:
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483:
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478:
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473:
470:
468:
467:Sacral dimple
465:
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458:
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237:) (next page)
236:
235:previous page
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218:previous page
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187:) (next page)
186:
185:previous page
182:
178:Subcategories
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56:
49:
48:
43:
34:
29:
25:
18:
17:
562:Strophosomia
339:Porencephaly
304:Pelvic digit
226:
207:(13 C, 49 P)
180:
58:
52:
45:
32:
651:Ulas family
517:Sirenomelia
820:Pediatrics
799:Categories
203:Teratogens
329:Polymelia
75:Contents
810:Genetics
584:Teratoma
63:disorder
55:medicine
42:category
67:birth
61:is a
57:, a
87:0–9
82:Top
53:In
44:is
801::
231:.
205:‎
69:.
788:(
771:Z
759:Y
747:X
710:W
673:V
646:U
574:T
455:S
393:R
274:P
242:O
233:(
216:(
192:T
183:(
167:Z
164:Y
161:X
158:W
155:V
152:U
149:T
146:S
143:R
140:Q
137:P
134:O
131:N
128:M
125:L
122:K
119:J
116:I
113:H
110:G
107:F
104:E
101:D
98:C
95:B
92:A
50:.
30:.
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