OMOP Concept 4305010
Opitz-Frias syndrome
StandardConditionSNOMED81771002Disorder
Maps from
3
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
3 source codes normalize to Opitz-Frias syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 131772 | Opitz-Frias Syndrome | Non-standard |
| MeSH | C567932 | Opitz GBBB Syndrome, X-Linked | Non-standard |
| Nebraska Lexicon | 81771002 | Hypertelorism-hypospadias syndrome | Non-standard |
Synonyms
Alternative names recorded for Opitz-Frias syndrome across source vocabularies.
- Congenital cleft larynx and Opitz-Frias syndrome
- G syndrome
- Hypertelorism-hypospadias syndrome
- Opitz-Frias syndrome (disorder)
- Opitz's (J.M.) syndrome
- Opitz syndrome
- síndrome de hipertelorismo - hipospadias
- síndrome de Opitz
- síndrome de Opitz - Frias
- síndrome de Opitz - Frias (trastorno)
- síndrome G
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(74)Roll up to these when you need a wider cohort.
- 1Congenital cleft larynx
- 1Developmental hereditary disorder
- 1Hereditary disorder of the urinary system
- 1Multiple malformation syndrome, moderate short stature, facial
- 1Penile hypospadias
- 1Reproductive system hereditary disorder
- 1Sex-linked hereditary disorder
- 2Congenital anomaly of larynx
- 2Congenital anomaly of penis
- 2Developmental disorder
- 2Disorder of reproductive system
- 2Disorder of urinary system
- 2Glans penis finding
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Hypospadias
- 2Lesion of larynx
- 2Multiple system malformation syndrome
- 3Congenital anomaly of anterior portion of neck
- 3Congenital anomaly of male genital system
- 3Congenital anomaly of upper respiratory system
- 3Congenital anomaly of urethra
- 3Congenital malformation syndrome
- 3Disease
- 3Disorder of body system
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