OMOP Concept 37396323
Schmitt Gillenwater Kelly syndrome
StandardConditionSNOMED716092007Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2016
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Schmitt Gillenwater Kelly syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C536262 | Radial hypoplasia, triphalangeal thumbs and hypospadias | Non-standard |
Synonyms
Alternative names recorded for Schmitt Gillenwater Kelly syndrome across source vocabularies.
- Radial hypoplasia and triphalangeal thumb with hypospadias and maxillary diastema syndrome
- Radial hypoplasia and triphalangeal thumb with hypospadias and maxillary diastema syndrome (disorder)
- síndrome de hipoplasia radial y pulgar trifalángico con hipospadias y diastema maxilar
- síndrome de hipoplasia radial y pulgar trifalángico con hipospadias y diastema maxilar (trastorno)
- síndrome de Schmitt Gillenwater Kelly
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(114)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Congenital hypoplasia of radius
- 1Developmental hereditary disorder
- 1Disorder of digestive system specific to fetus OR newborn
- 1Generalized spacing of maxillary teeth
- 1Hereditary disorder of musculoskeletal system
- 1Hereditary disorder of the urinary system
- 1Hereditary disorder of tooth
- 1Hypospadias
- 1Triphalangeal thumb
- 2Autosomal hereditary disorder
- 2Congenital anomaly of perineum
- 2Congenital anomaly of radius
- 2Congenital anomaly of urethra
- 2Congenital hypoplasia of bone of radius and/or ulna
- 2Developmental disorder
- 2Diastema of teeth
- 2Digestive system hereditary disorder
- 2Disorder of digestive system
- 2Disorder of musculoskeletal system
- 2Disorder of urinary system
- 2Fetal and/or neonatal disorder
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Hyperphalangy
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