OMOP Concept 4172984
Oto-palato-digital syndrome, type II
StandardConditionSNOMED42432003Disorder
Maps from
4
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
4 source codes normalize to Oto-palato-digital syndrome, type II via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 131106 | Oto-Palato-Digital Syndrome, Type II | Non-standard |
| MeSH | C538089 | Oto-palato-digital syndrome, type 2 | Non-standard |
| Nebraska Lexicon | 42432003 | Otopalatodigital syndrome | Non-standard |
| Read | PKy5700 | Otopalatodigital syndrome | Non-standard |
Synonyms
Alternative names recorded for Oto-palato-digital syndrome, type II across source vocabularies.
- Otopalatodigital syndrome type 2
- Oto-palato-digital syndrome, type II (disorder)
- síndrome otopalatodigital, tipo II
- síndrome otopalatodigital, tipo II (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(49)Roll up to these when you need a wider cohort.
- 1Auditory system hereditary disorder
- 1Cleft palate
- 1Congenital anomaly of face
- 1Congenital anomaly of limb
- 1Disorder of ear
- 1Otopalatodigital syndrome spectrum disorder
- 2Congenital anomaly of head
- 2Congenital anomaly of palate
- 2Congenital anomaly of skeletal bone
- 2Congenital malformation
- 2Developmental hereditary disorder
- 2Disorder of auditory system
- 2Disorder of face
- 2Disorder of head
- 2Disorder of limb
- 2Disorder of sensory organ
- 2Ear finding
- 2Ear, nose and throat disorder
- 2Hereditary disorder by system
- 2Hereditary disorder of musculoskeletal system
- 2Orofacial cleft
- 2Skeletal dysplasia
- 2X-linked dominant hereditary disease
- 3Congenital anomaly of musculoskeletal system
- 3Congenital disease
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