Knowledge (XXG)

Template:X-linked disorders

Source đź“ť

639: 822: 763: 654: 270: 796: 759: 650: 326: 190: 226: 37: 658: 86: 533: 381: 415: 452: 817: 528: 195: 171: 812: 371: 106: 745: 161: 447: 405: 231: 376: 311: 30: 673: 538: 792: 753: 646: 157: 480: 60: 562: 76: 81: 618: 543: 437: 91: 613: 200: 316: 573: 433: 96: 608: 275: 578: 502: 292: 221: 593: 442: 400: 350: 302: 244: 425: 257: 213: 139: 111: 410: 121: 583: 283: 181: 749: 475: 166: 149: 588: 462: 677: 523: 470: 346: 341: 262: 68: 603: 518: 391: 356: 288: 806: 687: 598: 361: 321: 249: 236: 134: 129: 101: 208: 46: 633: 715:
will show the template collapsed, i.e. hidden apart from its title bar.
680:), it is hidden apart from its title bar; if not, it is fully visible. 15: 672:, meaning that if there is another collapsible item on the page (a 494: 490: 331: 560: 58: 19: 784: 776: 772: 739:
will show the template expanded, i.e. fully visible.
823:
Genetic disease and disorder templates by mechanism
718: 694: 511: 489: 461: 424: 390: 301: 180: 148: 120: 67: 769:Editors can experiment in this template's sandbox 683:To change this template's initial visibility, the 237:Danon disease/glycogen storage disease Type IIb 342:Color blindness (red and green, but not blue) 327:Alpha-thalassemia mental retardation syndrome 31: 8: 227:Glucose-6-phosphate dehydrogenase deficiency 557: 55: 38: 24: 16: 667:initial visibility currently defaults to 87:X-linked severe combined immunodeficiency 481:X-linked nephrogenic diabetes insipidus 406:Hypohidrotic ectodermal dysplasia (EDA) 684: 416:X-linked endothelial corneal dystrophy 372:Charcot–Marie–Tooth disease (CMTX2-3) 196:Ornithine transcarbamylase deficiency 172:X-linked adrenal hypoplasia congenita 7: 678:table with the collapsible attribute 107:X-linked lymphoproliferative disease 77:Chronic granulomatous disease (CYBB) 453:Emery–Dreifuss muscular dystrophy 1 162:Spinal and bulbar muscular atrophy 14: 232:Pyruvate dehydrogenase deficiency 637: 312:X-linked intellectual disability 754:Template:X-linked disorders/doc 158:Androgen insensitivity syndrome 534:Simpson–Golabi–Behmel syndrome 1: 503:AMELX Amelogenesis imperfecta 443:Centronuclear myopathy (MTM1) 140:X-linked sideroblastic anemia 818:X-linked recessive disorders 529:Smith–Fineman–Myers syndrome 377:Pelizaeus–Merzbacher disease 271:Purine–pyrimidine metabolism 813:X-linked dominant disorders 619:Craniofrontonasal dysplasia 544:Nasodigitoacoustic syndrome 92:X-linked agammaglobulinemia 839: 743: 614:Orofaciodigital syndrome 1 448:Conradi–Hünermann syndrome 201:Oculocerebrorenal syndrome 797:Subpages of this template 574:X-linked hypophosphatemia 569: 556: 434:Becker muscular dystrophy 97:Hyper-IgM syndrome type 1 54: 539:Mohr–Tranebjærg syndrome 82:Wiskott–Aldrich syndrome 579:Focal dermal hypoplasia 293:Occipital horn syndrome 222:Carbohydrate metabolism 791:Add categories to the 642:Template documentation 594:Incontinentia pigmenti 401:Dyskeratosis congenita 245:Lipid storage disorder 167:KAL1 Kallmann syndrome 317:Coffin–Lowry syndrome 258:Mucopolysaccharidosis 609:Lujan–Fryns syndrome 276:Lesch–Nyhan syndrome 214:Adrenoleukodystrophy 112:Properdin deficiency 411:X-linked ichthyosis 723:X-linked disorders 699:X-linked disorders 584:Fragile X syndrome 394:and related tissue 61:X-linked recessive 631: 630: 627: 626: 563:X-linked dominant 552: 551: 512:No primary system 830: 788: 780: 767: 738: 737: 733: 730: 727: 724: 721: 714: 713: 709: 706: 703: 700: 697: 686: 685:|state= 670: 665:This template's 662: 643: 641: 640: 589:Aicardi syndrome 558: 56: 40: 33: 26: 17: 838: 837: 833: 832: 831: 829: 828: 827: 803: 802: 801: 800: 790: 782: 770: 768: 757: 742: 735: 731: 728: 725: 722: 719: 711: 707: 704: 701: 698: 695: 674:navbox, sidebar 668: 663: 644: 638: 636: 632: 623: 565: 548: 524:McLeod syndrome 507: 485: 471:Alport syndrome 457: 420: 386: 347:Ocular albinism 297: 263:Hunter syndrome 176: 144: 116: 63: 50: 44: 12: 11: 5: 836: 834: 826: 825: 820: 815: 805: 804: 781:and testcases 741: 740: 716: 635: 634: 629: 628: 625: 624: 622: 621: 616: 611: 606: 604:CHILD syndrome 601: 596: 591: 586: 581: 576: 570: 567: 566: 561: 554: 553: 550: 549: 547: 546: 541: 536: 531: 526: 521: 519:Barth syndrome 515: 513: 509: 508: 506: 505: 499: 497: 487: 486: 484: 483: 478: 476:Dent's disease 473: 467: 465: 459: 458: 456: 455: 450: 445: 440: 430: 428: 422: 421: 419: 418: 413: 408: 403: 397: 395: 388: 387: 385: 384: 379: 374: 365: 364: 359: 357:Norrie disease 354: 344: 339:Eye disorders: 335: 334: 329: 324: 319: 307: 305: 303:Nervous system 299: 298: 296: 295: 289:Menkes disease 279: 278: 266: 265: 253: 252: 240: 239: 234: 229: 217: 216: 204: 203: 198: 186: 184: 178: 177: 175: 174: 169: 164: 154: 152: 146: 145: 143: 142: 137: 132: 126: 124: 118: 117: 115: 114: 109: 104: 99: 94: 89: 84: 79: 73: 71: 65: 64: 59: 52: 51: 45: 43: 42: 35: 28: 20: 13: 10: 9: 6: 4: 3: 2: 835: 824: 821: 819: 816: 814: 811: 810: 808: 798: 794: 786: 778: 774: 765: 761: 755: 751: 747: 746:documentation 717: 693: 692: 691: 690:may be used: 689: 681: 679: 675: 671: 660: 656: 652: 648: 620: 617: 615: 612: 610: 607: 605: 602: 600: 599:Rett syndrome 597: 595: 592: 590: 587: 585: 582: 580: 577: 575: 572: 571: 568: 564: 559: 555: 545: 542: 540: 537: 535: 532: 530: 527: 525: 522: 520: 517: 516: 514: 510: 504: 501: 500: 498: 496: 492: 488: 482: 479: 477: 474: 472: 469: 468: 466: 464: 460: 454: 451: 449: 446: 444: 441: 439: 435: 432: 431: 429: 427: 426:Neuromuscular 423: 417: 414: 412: 409: 407: 404: 402: 399: 398: 396: 393: 389: 383: 380: 378: 375: 373: 370: 367: 366: 363: 362:Choroideremia 360: 358: 355: 352: 348: 345: 343: 340: 337: 336: 333: 330: 328: 325: 323: 322:MASA syndrome 320: 318: 315: 313: 309: 308: 306: 304: 300: 294: 290: 287: 285: 281: 280: 277: 274: 272: 268: 267: 264: 261: 259: 255: 254: 251: 250:Fabry disease 247: 246: 242: 241: 238: 235: 233: 230: 228: 225: 223: 219: 218: 215: 212: 210: 206: 205: 202: 199: 197: 194: 192: 188: 187: 185: 183: 179: 173: 170: 168: 165: 163: 159: 156: 155: 153: 151: 147: 141: 138: 136: 135:Haemophilia B 133: 131: 130:Haemophilia A 128: 127: 125: 123: 119: 113: 110: 108: 105: 103: 100: 98: 95: 93: 90: 88: 85: 83: 80: 78: 75: 74: 72: 70: 66: 62: 57: 53: 48: 41: 36: 34: 29: 27: 22: 21: 18: 682: 669:autocollapse 666: 664: 368: 338: 310: 282: 269: 256: 243: 220: 209:Dyslipidemia 207: 189: 23: 750:transcluded 657:] [ 653:] [ 649:] [ 122:Hematologic 807:Categories 744:The above 191:Amino acid 795:subpage. 710:collapsed 688:parameter 182:Metabolic 150:Endocrine 49:disorders 734:expanded 463:Urologic 438:Duchenne 47:X-linked 775:| 764:history 762:| 655:history 284:Mineral 789:pages. 785:create 777:mirror 773:create 369:Other: 69:Immune 752:from 729:state 705:state 676:, or 661:] 659:purge 645:[ 495:tooth 382:SMAX2 793:/doc 760:edit 651:edit 647:view 491:Bone 392:Skin 332:PHF8 102:IPEX 748:is 809:: 756:. 736:}} 720:{{ 712:}} 696:{{ 248:: 799:. 787:) 783:( 779:) 771:( 766:) 758:( 732:= 726:| 708:= 702:| 493:/ 436:/ 353:) 351:1 349:( 314:: 291:/ 286:: 273:: 260:: 224:: 211:: 193:: 160:/ 39:e 32:t 25:v

Index

v
t
e
X-linked
X-linked recessive
Immune
Chronic granulomatous disease (CYBB)
Wiskott–Aldrich syndrome
X-linked severe combined immunodeficiency
X-linked agammaglobulinemia
Hyper-IgM syndrome type 1
IPEX
X-linked lymphoproliferative disease
Properdin deficiency
Hematologic
Haemophilia A
Haemophilia B
X-linked sideroblastic anemia
Endocrine
Androgen insensitivity syndrome
Spinal and bulbar muscular atrophy
KAL1 Kallmann syndrome
X-linked adrenal hypoplasia congenita
Metabolic
Amino acid
Ornithine transcarbamylase deficiency
Oculocerebrorenal syndrome
Dyslipidemia
Adrenoleukodystrophy
Carbohydrate metabolism

Text is available under the Creative Commons Attribution-ShareAlike License. Additional terms may apply.

↑