OMOP Concept 36714971
Acro-oto-ocular syndrome
StandardConditionSNOMED720410001Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Acro-oto-ocular syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C564866 | Acrootoocular Syndrome | Non-standard |
| Nebraska Lexicon | 720410001 | Pseudopapilloedema, blepharophimosis and hand anomaly syndrome | Non-standard |
Synonyms
Alternative names recorded for Acro-oto-ocular syndrome across source vocabularies.
- Acrootoocular syndrome
- Acrootoocular syndrome (disorder)
- Pseudopapilledema, blepharophimosis and hand anomaly syndrome
- Pseudopapilloedema, blepharophimosis and hand anomaly syndrome
- síndrome acro-oto-ocular
- síndrome acro-oto-ocular (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(51)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Developmental hereditary disorder
- 1Inherited optic neuropathy
- 1Multiple malformation syndrome with facial-limb defects as major feature
- 1Pseudopapilledema
- 2Autosomal hereditary disorder
- 2Congenital anomaly of limb
- 2Developmental disorder
- 2Disorder of optic nerve
- 2Hereditary disease
- 2Hereditary disorder of nervous system
- 2Hereditary disorder of the visual system
- 2Multiple malformation syndrome with facial defects as major feature
- 2Multiple malformation syndrome with limb defect as major feature
- 2Optic disc disorder
- 3Congenital anomaly of face
- 3Congenital malformation
- 3Cranial nerve disorder
- 3Disease
- 3Disorder of limb
- 3Disorder of nervous system
- 3Disorder of visual pathways
- 3Genetic disease
- 3Hereditary disorder by system
- 3Multiple system malformation syndrome
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