Informaţii despre

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

Vezi şi

Boli A-Z Albinism, Oculocutaneous, Type Ii Angelman Syndrome Chromosomal Disease Juvenile Hereditary Hemochromatosis Prader-Willi-Like Syndrome Due to a Point Mutation Prader-Willi Syndrome 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 Translocation