Knowledge (XXG)

Gastrocutaneous syndrome

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37: 272: 141: 176: 265: 301: 258: 87: 187: 291: 216: 82: 108:"Gastrocutaneous syndrome | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program" 296: 66: 137: 49: 242: 30:
Peptic ulcer/hiatal hernia, multiple lentigines/cafe-au-lait spots, hypertelorism, myopia
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Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007).
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Gastrocutaneous syndrome is an autosomal dominant disorder.
246: 158: 202: 162: 48: 26: 21: 69:cutaneous condition characterized by multiple 266: 8: 273: 259: 159: 35: 18: 99: 7: 234: 232: 245:. You can help Knowledge (XXG) by 14: 1: 88:List of cutaneous conditions 318: 231: 134:Dermatology: 2-Volume Set 112:rarediseases.info.nih.gov 43: 34: 63:Gastrocutaneous syndrome 22:Gastrocutaneous syndrome 302:Genodermatoses stubs 136:. St. Louis: Mosby. 203:External resources 83:Gardner's syndrome 67:autosomal dominant 254: 253: 226: 225: 143:978-1-4160-2999-1 60: 59: 16:Medical condition 309: 275: 268: 261: 233: 160: 148: 147: 129: 123: 122: 120: 118: 104: 39: 19: 317: 316: 312: 311: 310: 308: 307: 306: 282: 281: 280: 279: 229: 227: 222: 221: 198: 197: 171: 157: 152: 151: 144: 131: 130: 126: 116: 114: 106: 105: 101: 96: 79: 17: 12: 11: 5: 315: 313: 305: 304: 299: 294: 292:Genodermatoses 284: 283: 278: 277: 270: 263: 255: 252: 251: 239:Genodermatoses 224: 223: 220: 219: 207: 206: 204: 200: 199: 196: 195: 184: 172: 167: 166: 164: 163:Classification 156: 155:External links 153: 150: 149: 142: 124: 98: 97: 95: 92: 91: 90: 85: 78: 75: 58: 57: 52: 46: 45: 41: 40: 32: 31: 28: 24: 23: 15: 13: 10: 9: 6: 4: 3: 2: 314: 303: 300: 298: 295: 293: 290: 289: 287: 276: 271: 269: 264: 262: 257: 256: 250: 248: 244: 241:article is a 240: 235: 230: 218: 214: 213: 209: 208: 205: 201: 194: 190: 189: 185: 183: 179: 178: 174: 173: 170: 165: 161: 154: 145: 139: 135: 128: 125: 113: 109: 103: 100: 93: 89: 86: 84: 81: 80: 76: 74: 72: 68: 64: 56: 53: 51: 47: 42: 38: 33: 29: 25: 20: 247:expanding it 236: 228: 210: 186: 175: 133: 127: 115:. Retrieved 111: 102: 62: 61: 55:Dermatology 27:Other names 286:Categories 94:References 71:lentigines 65:is a rare 297:Syndromes 50:Specialty 212:Orphanet 117:17 March 77:See also 193:C535651 182:137270 140:  237:This 243:stub 217:2069 188:MeSH 177:OMIM 138:ISBN 119:2019 288:: 215:: 191:: 180:: 110:. 73:. 274:e 267:t 260:v 249:. 169:D 146:. 121:.

Index


Specialty
Dermatology
autosomal dominant
lentigines
Gardner's syndrome
List of cutaneous conditions
"Gastrocutaneous syndrome | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program"
ISBN
978-1-4160-2999-1
D
OMIM
137270
MeSH
C535651
Orphanet
2069
Genodermatoses
stub
expanding it
v
t
e
Categories
Genodermatoses
Syndromes
Genodermatoses stubs

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