Informaţii despre
| Nume | Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type 1 | |
|---|---|---|
| Pagina Web | www.malacards.org | |
| Clasificare globală Malacards | Boli fetale; Boli genetice; Boli rare | |
| Clasificari ICD10 | Congenital malformation syndromes predominantly associated with short stature | |
| Clasificare anatomică Malacards | Boli ale sistemului reproducator; Boli endocrine; Boli neuronale | |
| Boli din aceeaşi familie | Prader-Willi Syndrome Due to Imprinting Mutation; Prader-Willi Syndrome Due to Maternal Uniparental Disomy of Chromosome 15; Prader-Willi Syndrome Due to Paternal 15q11q13 Deletion; Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type 2; Prader-Willi Syndrome Due to Translocation; Prader-Willi-Like Syndrome Due to a Point Mutation |