OMOP Concept 36714634
Oliver McFarlane syndrome
StandardConditionSNOMED719944006Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
2 source codes normalize to Oliver McFarlane syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C536554 | Oliver-McFarlane syndrome | Non-standard |
| Nebraska Lexicon | 719944006 | Trichomegaly with retina pigmentary degeneration and dwarfism syndrome | Non-standard |
Synonyms
Alternative names recorded for Oliver McFarlane syndrome across source vocabularies.
- síndrome de tricomegalia con degeneración del epitelio pigmentario de la retina y enanismo
- síndrome de tricomegalia con degeneración del epitelio pigmentario de la retina y enanismo (trastorno)
- Trichomegaly with retina pigmentary degeneration and dwarfism syndrome
- Trichomegaly with retina pigmentary degeneration and dwarfism syndrome (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(77)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Congenital anomaly of hair
- 1Congenital anomaly of retina
- 1Congenital deformity of face
- 1Congenital deformity of soft tissue
- 1Congenital structural abnormality of eyelid
- 1Deformity of eyelid
- 1Degeneration of retina
- 1Developmental hereditary disorder
- 1Disorder of hair growth
- 1Ectodermal dysplasia
- 1Hereditary disorder of the integument
- 1Hereditary disorder of the visual system
- 1Short stature disorder
- 2Autosomal hereditary disorder
- 2Congenital anomaly of face
- 2Congenital anomaly of ocular adnexa
- 2Congenital anomaly of posterior segment of eye
- 2Congenital anomaly of skin
- 2Congenital deformity
- 2Congenital ectodermal defect
- 2Deformity
- 2Deformity of tissue
- 2Degenerative disorder of eye
- 2Developmental disorder
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