Prader-Willi syndrome due to point mutation (Q48789662)

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human disease
  • Prader-Willi syndrome due to a point mutation
  • PWS due to point mutation
  • SCHAAF-YANG SYNDROME; SHFYNG
  • Prader-Willi-Like Syndrome
  • Schaaf-Yang syndrome
  • PWS due to a point mutation
  • SHFYNG
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Language Label Description Also known as
English
Prader-Willi syndrome due to point mutation
human disease
  • Prader-Willi syndrome due to a point mutation
  • PWS due to point mutation
  • SCHAAF-YANG SYNDROME; SHFYNG
  • Prader-Willi-Like Syndrome
  • Schaaf-Yang syndrome
  • PWS due to a point mutation
  • SHFYNG

Statements

Identifiers

 
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