OMOP Concept 37164244
SIM1-related Prader-Willi-like syndrome
StandardConditionSNOMED1229943004Disorder
Maps from
0
Descendants
0
Valid from
31 May 2022
Valid to
31 Dec 2099
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Synonyms
Alternative names recorded for SIM1-related Prader-Willi-like syndrome across source vocabularies.
- SIM bHLH transcription factor 1-related Prader-Willi-like syndrome
- SIM bHLH transcription factor 1-related Prader-Willi-like syndrome (disorder)
- síndrome similar a Prader Willi asociado al gen del factor de transcripción bHLH SIM 1
- síndrome similar a Prader Willi asociado al gen del factor de transcripción bHLH SIM 1 (trastorno)
- síndrome similar a Prader Willi asociado al gen SIM1
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(46)Roll up to these when you need a wider cohort.
- 1Prader-Willi-like syndrome
- 2Congenital hypogonadotropic hypogonadism
- 2Genetic disease
- 2Multiple malformation syndrome with facial defects as major feature
- 2Multiple malformation syndrome with unusual brain and/or neuromuscular findings
- 2Obesity
- 3Congenital anomaly of face
- 3Congenital disease
- 3Disease
- 3Hypogonadotropic hypogonadism
- 3Multiple system malformation syndrome
- 3Obese
- 4Clinical finding
- 4Congenital anomaly of head
- 4Congenital malformation syndrome
- 4Disorder of anterior pituitary
- 4Disorder of face
- 4Disorder of fetus and/or newborn
- 4High body weight
- 4Hypogonadism
- 4Hypopituitarism
- 5Congenital malformation
- 5Disorder of endocrine gonad
- 5Disorder of head
- 5Disorder of pituitary gland
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