MAGEL2-related Prader-Willi-like syndrome

Source codes that map to this concept

1 source code normalizes to MAGEL2-related Prader-Willi-like syndrome via the OMOP "Maps to" relationship.

Synonyms

Alternative names recorded for MAGEL2-related Prader-Willi-like syndrome across source vocabularies.

• MAGE family member L2-related Prader-Willi-like syndrome
• MAGE family member L2-related Prader-Willi-like syndrome (disorder)
• Schaaf Yang syndrome
• síndrome de Schaaf Yang
• síndrome de tipo Prader Willi asociado al miembro L2 de la familia de proteínas del gen de antígeno asociado a melanoma
• síndrome de tipo Prader Willi asociado al miembro L2 de la familia de proteínas del gen de antígeno asociado a melanoma (trastorno)
• síndrome de tipo Prader Willi asociado a MAGEL2

Where it sits in the hierarchy

Ordered by distance - 1 is a direct parent or child.

Get this concept via the API

Resolve MAGEL2-related Prader-Willi-like syndrome - and every code that maps to it - over HTTPS, against the current vocabulary release. No downloads, no local database.

curl "https://api.omophub.com/v1/concepts/37164247?include_relationships=true" \
  -H "Authorization: Bearer $OMOPHUB_API_KEY"