OMOP Concept 4082514
Imperfect fusion of skull
StandardConditionSNOMED23939000Disorder
Maps from
2
Descendants
90
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Imperfect fusion of skull via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 137701 | Imperfect fusion of skull | Non-standard |
| Read | PG06.00 | Imperfect fusion of skull | Non-standard |
Synonyms
Alternative names recorded for Imperfect fusion of skull across source vocabularies.
- fusión imperfecta del cráneo
- fusión imperfecta del cráneo (trastorno)
- Imperfect fusion of skull (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(21)Roll up to these when you need a wider cohort.
- 1Congenital anomaly of head
- 1Congenital anomaly of joint
- 1Cranial suture finding
- 1Lesion of joint
- 2Arthropathy
- 2Congenital anomaly of musculoskeletal system
- 2Congenital malformation
- 2Disorder of head
- 2Head finding
- 2Joint finding
- 2Structural abnormality of skeleton
- 3Clinical finding
- 3Congenital disease
- 3Developmental disorder
- 3Disease
- 3Disorder of joint region
- 3Disorder of musculoskeletal system
- 3Disorder of skeletal system
- 3Musculoskeletal finding
- 4Disorder of body system
- 4Fetal and/or neonatal disorder
Narrower concepts
(90)Included automatically when you query with descendants.
- 1Craniosynostosis syndrome
- 2Acrocephalosyndactyly
- 2Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome
- 2Baller-Gerold syndrome
- 2Complex craniosynostosis
- 2Congenital synostosis of coronal suture of skull
- 2Craniofacial dyssynostosis syndrome
- 2Craniofrontonasal dysplasia with Poland anomaly syndrome
- 2Craniomicromelic syndrome
- 2Craniorhiny
- 2Craniosynostosis, anal anomaly, porokeratosis syndrome
- 2Craniosynostosis and dental anomalies syndrome
- 2Craniosynostosis and intracranial calcification syndrome
- 2Craniosynostosis Boston type
- 2Craniosynostosis, facial dysmorphism, Chiari-1 malformation, developmental and language delay syndrome
- 2Craniosynostosis Herrmann Opitz type
- 2Craniosynostosis, microretrognathia, severe intellectual disability syndrome
- 2Craniosynostosis Philadelphia type
- 2Craniosynostosis with Dandy-Walker malformation and hydrocephalus syndrome
- 2Crouzon syndrome
- 2Curry Jones syndrome
- 2Cutis gyrata syndrome of Beare and Stevenson
- 2FGFR2-related bent bone dysplasia
- 2Fibroblast growth factor receptor 3-related craniosynostosis
- 2Holoprosencephaly craniosynostosis syndrome
Showing 25 of 90. Retrieve the full set via the API.
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