Índice de enfermedades genéticas ofrecidas por AC Gen Reading Life
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Busca la enfermedad o gen a estudiar (Recomendable en inglés) |
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A - B - C - D - E - F - G - H - I - J - K - L - M - N - O - P - Q - R - S - T - U - V - W - X - Y - Z
| Enfermedad/Phenotype | Phenotype MIM number | Simbolo del Gen | Nombre del Gen |
| Waardenburg syndrome, type 1 | 193500 | PAX3 | paired box 3 |
| Waardenburg syndrome, type 3 | 148820 | PAX3 | paired box 3 |
| Waardenburg syndrome/albinism, digenic | 103470 | TYR | tyrosinase |
| Warfarin sensitivity | 122700 | F9 | coagulation factor IX |
| Watson syndrome | 193520 | NF1 | neurofibromin 1 |
| Weaver syndrome | 277590 | NSD1 | nuclear receptor binding SET domain protein 1 |
| Weill-Marchesani syndrome 2, dominant | 608328 | FBN1 | fibrillin 1 |
| Weissenbacher-Zweymuller syndrome | 277610 | COL11A2 | collagen, type XI, alpha 2 |
| Werner syndrome | 277700 | WRN | Werner syndrome, RecQ helicase-like |
| Wilms tumor | |||
| Wilms tumor, somatic | 194070 | GPC3 | glypican 3 |
| Wilms tumor, type 1 | 194070 | WT1 | Wilms tumor 1 |
| Wilson disease | 277900 | ATP7B | ATPase, Cu++ transporting, beta polypeptide |
| Wiskott-Aldrich syndrome | 301000 | WAS | Wiskott-Aldrich syndrome |
| Wolff-Parkinson-White syndrome | 194200 | PRKAG2 | protein kinase, AMP-activated, gamma 2 non-catalytic subunit |
