Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1
Name: |
Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1
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ORPHAcode: |
177901
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XREF(s): | |
Analyte(s): | |
Created: |
13 May 2019 - 01:02
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Changed: |
22 Jun 2023 - 16:14
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