Knowledge (XXG)

Orofaciodigital syndrome

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in between 1 in 50,000 to 250,000 newborns with the majority of cases being type I (
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is a group of at least 13 related conditions that affect the development of the
415: 371: 441: 383: 348: 333: 318: 303: 288: 273: 258: 243: 228: 187:"Oral-facial-digital syndrome - Genetics Home Reference" 457: 361: 406: 365: 48: 26: 21: 156:Type IX, OFD syndrome with retinal abnormalities 477: 8: 304:OROFACIODIGITAL SYNDROME VIII; OFD8 - 300484 349:OROFACIODIGITAL SYNDROME XI; OFD11 - 612913 334:OROFACIODIGITAL SYNDROME X; OFD10 - 165590 289:OROFACIODIGITAL SYNDROME VII; OFD7 - 608518 484: 470: 362: 319:OROFACIODIGITAL SYNDROME IX; OFD9 - 258865 274:OROFACIODIGITAL SYNDROME VI; OFD6 - 277170 244:OROFACIODIGITAL SYNDROME IV; OFD4 - 258860 201:"National Organization for Rare Disorders" 147:Oral-facial-digital syndrome, Edwards type 63: 35: 18: 259:OROFACIODIGITAL SYNDROME V; OFD5 - 174300 178: 7: 438: 436: 345:Online Mendelian Inheritance in Man 330:Online Mendelian Inheritance in Man 315:Online Mendelian Inheritance in Man 300:Online Mendelian Inheritance in Man 285:Online Mendelian Inheritance in Man 270:Online Mendelian Inheritance in Man 255:Online Mendelian Inheritance in Man 240:Online Mendelian Inheritance in Man 225:Online Mendelian Inheritance in Man 456:. You can help Knowledge (XXG) by 44:Tongue in orofaciodigital syndrome 14: 440: 111:Papillon-League-Psaume syndrome 95:Papillon-League-Psaume syndrome 1: 136:Type VI, Varadi-Papp syndrome 79:oral-facial-digital syndrome 529: 435: 105:The different types are:s 508:Syndromes affecting teeth 149:(not to be confused with 43: 34: 75:Orofaciodigital syndrome 30:Orofaciodigital syndrome 22:Orofaciodigital syndrome 126:Baraitser-Burn syndrome 513:Genetic disorder stubs 229:MOHR SYNDROME - 252100 115:Type II, Mohr syndrome 407:External resources 167:Gabrielli syndrome 465: 464: 430: 429: 159:Type X, OFD with 132:Thurston syndrome 120:Sugarman syndrome 72: 71: 16:Medical condition 520: 486: 479: 472: 450:genetic disorder 444: 437: 363: 351: 342: 336: 327: 321: 312: 306: 297: 291: 282: 276: 267: 261: 252: 246: 237: 231: 222: 216: 215: 213: 212: 203:. Archived from 197: 191: 190: 183: 151:Edwards syndrome 68: 67: 59:medical genetics 39: 19: 528: 527: 523: 522: 521: 519: 518: 517: 493: 492: 491: 490: 433: 431: 426: 425: 402: 401: 374: 360: 355: 354: 343: 339: 328: 324: 313: 309: 298: 294: 283: 279: 268: 264: 253: 249: 238: 234: 223: 219: 210: 208: 199: 198: 194: 185: 184: 180: 175: 161:fibular aplasia 141:Whelan syndrome 103: 87:facial features 62: 17: 12: 11: 5: 526: 524: 516: 515: 510: 505: 503:Rare syndromes 495: 494: 489: 488: 481: 474: 466: 463: 462: 445: 428: 427: 424: 423: 411: 410: 408: 404: 403: 400: 399: 388: 375: 370: 369: 367: 366:Classification 359: 358:External links 356: 353: 352: 337: 322: 307: 292: 277: 262: 247: 232: 217: 192: 177: 176: 174: 171: 170: 169: 163: 157: 154: 143: 137: 134: 128: 122: 116: 113: 102: 99: 70: 69: 52: 46: 45: 41: 40: 32: 31: 28: 24: 23: 15: 13: 10: 9: 6: 4: 3: 2: 525: 514: 511: 509: 506: 504: 501: 500: 498: 487: 482: 480: 475: 473: 468: 467: 461: 459: 455: 452:article is a 451: 446: 443: 439: 434: 422: 418: 417: 413: 412: 409: 405: 398: 394: 393: 389: 386: 385: 381: 377: 376: 373: 368: 364: 357: 350: 346: 341: 338: 335: 331: 326: 323: 320: 316: 311: 308: 305: 301: 296: 293: 290: 286: 281: 278: 275: 271: 266: 263: 260: 256: 251: 248: 245: 241: 236: 233: 230: 226: 221: 218: 207:on 2014-08-16 206: 202: 196: 193: 188: 182: 179: 172: 168: 164: 162: 158: 155: 152: 148: 144: 142: 138: 135: 133: 129: 127: 123: 121: 117: 114: 112: 108: 107: 106: 100: 98: 96: 92: 88: 84: 80: 76: 66: 60: 56: 53: 51: 47: 42: 38: 33: 29: 25: 20: 458:expanding it 447: 432: 414: 390: 378: 340: 325: 310: 295: 280: 265: 250: 235: 220: 209:. Retrieved 205:the original 195: 181: 104: 78: 74: 73: 55:Rheumatology 145:Type VIII, 27:Other names 497:Categories 211:2015-03-02 173:References 139:Type VII, 118:Type III, 165:Type XI, 124:Type IV, 50:Specialty 416:Orphanet 347:(OMIM): 332:(OMIM): 317:(OMIM): 302:(OMIM): 287:(OMIM): 272:(OMIM): 257:(OMIM): 242:(OMIM): 227:(OMIM): 130:Type V, 109:Type I, 397:D009958 387:: Q87.0 421:140997 91:digits 89:, and 61:  448:This 83:mouth 454:stub 392:MeSH 101:Type 380:ICD 97:). 77:or 499:: 419:: 395:: 384:10 85:, 57:, 485:e 478:t 471:v 460:. 382:- 372:D 214:. 189:. 153:)

Index


Specialty
Rheumatology
medical genetics
Edit this on Wikidata
mouth
facial features
digits
Papillon-League-Psaume syndrome
Papillon-League-Psaume syndrome
Sugarman syndrome
Baraitser-Burn syndrome
Thurston syndrome
Whelan syndrome
Oral-facial-digital syndrome, Edwards type
Edwards syndrome
fibular aplasia
Gabrielli syndrome
"Oral-facial-digital syndrome - Genetics Home Reference"
"National Organization for Rare Disorders"
the original
Online Mendelian Inheritance in Man
MOHR SYNDROME - 252100
Online Mendelian Inheritance in Man
OROFACIODIGITAL SYNDROME IV; OFD4 - 258860
Online Mendelian Inheritance in Man
OROFACIODIGITAL SYNDROME V; OFD5 - 174300
Online Mendelian Inheritance in Man
OROFACIODIGITAL SYNDROME VI; OFD6 - 277170
Online Mendelian Inheritance in Man

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