Application Version: 4.0.6.4
Content Version: 2021.03.26
Release Notes [PDF272KB]
User Guide [PDF6.08MB]
Code System Update Calendar [PDF112KB] ![]()
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Value Set Information
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Version History
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- Value Set Concepts
- Value Set Details
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| Concept Code | Concept Name | Preferred Concept Name | Code System | Value Set | ||
|---|---|---|---|---|---|---|
| 86268005 | Achondroplasia (disorder) | Achondroplasia (disorder) | SNOMED-CT | Family History (HW) | Details | |
| 63702009 | Alstrom syndrome (disorder) | Alstrom syndrome (disorder) | SNOMED-CT | Family History (HW) | Details | |
| 195967001 | Asthma (disorder) | Asthma (disorder) | SNOMED-CT | Family History (HW) | Details | |
| 5619004 | Bardet-Biedl syndrome (disorder) | Bardet-Biedl syndrome (disorder) | SNOMED-CT | Family History (HW) | Details | |
| 81780002 | Beckwith-Wiedemann syndrome (disorder) | Beckwith-Wiedemann syndrome (disorder) | SNOMED-CT | Family History (HW) | Details | |
| 162863004 | Body mass index 25-29 - overweight (finding) | Body mass index 25-29 - overweight (finding) | SNOMED-CT | Family History (HW) | Details | |
| 162864005 | Body mass index 30+ - obesity (finding) | Body mass index 30+ - obesity (finding) | SNOMED-CT | Family History (HW) | Details | |
| 21634003 | Borjeson-Forssman-Lehmann syndrome (disorder) | Borjeson-Forssman-Lehmann syndrome (disorder) | SNOMED-CT | Family History (HW) | Details | |
| 405617006 | Cardiovascular event (event) | Cardiovascular event (event) | SNOMED-CT | Family History (HW) | Details | |
| 205813009 | Carpenter's syndrome (disorder) | Carpenter's syndrome (disorder) | SNOMED-CT | Family History (HW) | Details | |
| 128188000 | Cerebral palsy (disorder) | Cerebral palsy (disorder) | SNOMED-CT | Family History (HW) | Details | |
| 444862003 | Childhood obesity (disorder) | Childhood obesity (disorder) | SNOMED-CT | Family History (HW) | Details | |
| 56604005 | Cohen syndrome (disorder) | Cohen syndrome (disorder) | SNOMED-CT | Family History (HW) | Details | |
| 41040004 | Complete trisomy 21 syndrome (disorder) | Complete trisomy 21 syndrome (disorder) | SNOMED-CT | Family History (HW) | Details | |
| 40354009 | De Lange syndrome (disorder) | De Lange syndrome (disorder) | SNOMED-CT | Family History (HW) | Details | |
Application Version: 4.0.6.4
Content Version: 2021.03.26
Release Notes [PDF272KB]
User Guide [PDF6.08MB]
Code System Update Calendar [PDF112KB] ![]()
Contact Us
Subscribe
Related Links
- PHIN Vocabulary Services
- Quick Links / Mapping Tools
- External Standards Resources
- Message Guides
- Developer's Guide
Downloads
- Page last reviewed:December 5, 2018
- Page last updated:December 5, 2018
- Content source:


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