Informaţii despre
Nume | Prader-Willi-Like Syndrome Due to a Point Mutation | |
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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 1; Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type 2; Prader-Willi Syndrome Due to Translocation |