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SNOMED CT
Acronym | SNOMEDCT |
Visibility | Public |
Description | The US Edition of SNOMED CT combines the International Release of SNOMED CT and the US Extension of SNOMED CT SNOMED CT provides the core general terminology for the electronic health record (EHR). The concepts have unique meanings and formal logic-based definitions organized into hierarchies. Each International Release includes the core of the terminology (concepts, descriptions, and relationships), together with works to support the implementation and use of SNOMED CT, including subsets, cross maps to existing classifications and coding schemes, and an extensive set of guidelines. The US Extension to SNOMED CT included the concepts, descriptions, and relationships accepted by NLM as a formal extension to the SNOMED CT International Release. NLM no longer releases the standalone US Extension. The US Edition of SNOMED CT includes more than 300,000 unique concepts. There are over 1,000,000 descriptions in SNOMED CT, including synonyms that can be used to refer to a concept. In addition, there are approximately 903,000 links or semantic relationships between the SNOMED CT concepts. |
Status | Production |
Format | UMLS |
Contact | NLM Customer Service, custserv@nlm.nih.gov |
Categories | Health |
Groups | Cancer Biomedical Informatics Grid, Unified Medical Language System |
License Information | This ontology is made available via the UMLS. Users of all UMLS ontologies must abide by the terms of the UMLS license. |
Version | Released | Uploaded |
---|---|---|
SNOMEDCT_US_2024_09_01 (Parsed, Indexed, Metrics, Annotator, Error Diff) | 11/04/2024 | 01/16/2025 |
2024AA (Archived) | 05/06/2024 | 08/28/2024 |
2023AB (Archived) | 11/06/2023 | 01/31/2024 |
2023AA (Archived) | 04/01/2023 | 08/07/2023 |
2022AB (Archived) | 11/07/2022 | 01/06/2023 |
2022AA (Archived) | 05/02/2022 | 06/10/2022 |
2021AB (Archived) | 11/01/2021 | 11/18/2021 |
2021AA (Archived) | 04/03/2021 | 05/20/2021 |
2020AB (Archived) | 11/02/2020 | 01/06/2021 |
2020AA (Archived) | 05/04/2018 | 09/24/2020 |
2019AB (Archived) | 11/04/2019 | 11/18/2019 |
2019AA (Archived) | 05/06/2019 | 08/27/2019 |
2018AB (Archived) | 11/05/2018 | 04/29/2019 |
2018AA (Archived) | 05/07/2018 | 07/06/2018 |
2017AB (Archived) | 11/06/2017 | 07/06/2018 |
2017AA (Archived) | 05/08/2017 | 04/06/2018 |
2016AB (Archived) | 02/06/2017 | 02/06/2017 |
2016AA (Archived) | 09/06/2016 | 09/06/2016 |
2015AB (Archived) | 07/20/2016 | 07/20/2016 |
2015AA (Archived) | 06/09/2015 | 06/09/2015 |
2014AB (Archived) | 01/29/2015 | 01/29/2015 |
2014AA (Archived) | 02/21/2014 | 02/21/2014 |
2013AA (Archived) | 02/18/2014 | 02/18/2014 |
2013AA (Archived) | 01/14/2014 | 01/14/2014 |
2013AA (Archived) | 05/08/2013 | 09/25/2013 |
2011_01_31 (Archived) | 01/31/2011 | 08/11/2011 |
2010_07_31 (Archived) | 07/31/2010 | 11/09/2010 |
2010_01_31 (Archived) | 01/31/2010 | 05/12/2010 |
2009_07_31 (Archived) | 07/31/2009 | 01/05/2010 |
2009_01_31 (Archived) | 01/31/2009 | 07/31/2009 |
more... |
- CCC Nursing Ontology
- This is nursing diagnosis ontology of Clinical Care Classification
- Cardiac-centered Frailty Ontology
- This ontology is designed to cover the portions of reality relevant to assessing patient frailty. While we believe it to be relevant to frailty in general, during its development we were specifically focused on decisions relating to cardiac care. We gathered terms using existent instruments, physician interviews, and automated chart reviews. The hierarchical structure was taken from SNOMED-CT. We could not simply use SNOMED-CT because it is too exhaustive to be useful. We add entities where necessary to remain true to our data.
- Drug-Induce Liver Injury (combined)
- A SNOMED subset of terms related to histological and clinical descriptions of Drug Induced Liver Injury (DILI). See Wang et al., "A Unifying Ontology to Integrate Histological and Clinical Observations for Drug-Induce Liver Injury" The American Journal of Pathology, 182:4,1180-1187 (2013). This view contains both of the DILIo major branches; SNOMED:Body Structure and SNOMED:Clinical finding Some of the class names have been changed to correspond to the preferred names in SNOMED of 7/31/2011. In DILIo publication -> in this file; Disorder of liver -> Disease of liver; Finding of general form of body -> General form of body - finding; Finding of size of liver -> size of liver - finding; Subacute necrosis of liver -> subacute hepatic necrosis
- Maternity_Test_Case2
- Testing
- MEdical LifeLog Ontology for people with disability
- No description provided
- SNOMED CT Standard Ontology Based on the Ontology for General Medical Science
- The Systematized Nomenclature of Medicine Clinical Term Ontology (SCTO) attempts to create a basic OWL 2 ontology for SNOMED CT terminology. The ontology is built based on the Ontology of General Medical Science (OGMS). This ontology implements the SNOMED CT concept model by adding the appropriate axioms to its top-level concepts. The resulting ontology can prevent redundancies and inconsistencies in this large terminology. Moreover, the terminology maintenance can become more accurate. Finally, SNOMED CT can be used in a healthcare environment to create more complex post-coordinated expressions and constraints in a more accurate manner.
- SNOMED Terminos Clinicos
- SNOMED Terminos Clinicos (SNOMED CT), Edicion en Espanol, Distribucion Internacional, Octubre de 2008, 2009_04_30
- Neoplasm_hamartoma
- subset of snomed-ct regarding neoplasm and hamartoma
- Neoplasm_breast_cancer
- This a subset of Neoplasm_hamartoma view, based on Snomed clinical practice's used terms (Fondazione S.Maugeri anatomic pathology dep.). This subset is not to be meant exhaustive, it has been created in order to built a proper ontology for our project, ONCO-i2b2, through the NCBO Ontology Tools.
- Snomed neoplasm, breast cancer
- This a subset of snomed-ct regarding neoplasm and hamartoma, based on Snomed clinical practice's used terms (Fondazione S.Maugeri anatomic pathology dep.). This subset is not to be meant exhaustive, it has been created in order to built a proper ontology for our project, ONCO-i2b2, through the NCBO Ontology Tools.
- Snomed, Body Structure
- The Body Structure subtree in SNOMED-CT. It has been created in order to built a proper ontology for our project, ONCO-i2b2, through the NCBO Ontology Tools.
- SNOMED Ethnic Group
- Ethnic Group From SNOMED CT
- SNOMED Anatomy
- The Anatomy class subtree in SNOMED-CT based on SNOMED CT 2009.07.31
- SNOMED Clinical Finding
- Extract from SNOMED
- SNOMED Organism
- The Organism subtree in SNOMED-CT based on SNOMED-CT v. 2009.01.31
- SNOMED Test Findings
- The Test Findings subtree in SNOMED-CT based on SNOMED-CT v. 2009.01.31
- SNOMED Morphologically Abnormal Structure
- The Morphologically Abnormal Structure subtree of SNOMED CT
- Reserved Acronym SNOMEDCT_US
- Reserved acronym to prevent URI collusion with SNOMEDCT. see https://github.com/ncbo/bioportal-project/issues/198
Classes | 375,783 |
Individuals | 0 |
Properties | 246 |
Maximum depth | 30 |
Maximum number of children | 3,027 |
Average number of children | 4 |
Classes with a single child | 48,683 |
Classes with more than 25 children | 3,114 |
Classes with no definition | 367,146 |
Educatioal Medical Materials Annotator
International Fanconi Anemia Registry
Mapping of Norwegian national quality registries- Variabelbibliotek for medisinske kvalitetsregistre
Nomenclature for Anatomic Pathology
Rehabilita, Disruptive Technologies for the Rehabilitation of the Future
Id | http://purl.bioontology.org/ontology/SNOMEDCT/56558005
http://purl.bioontology.org/ontology/SNOMEDCT/56558005
|
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Preferred Name | Congenital hypotrichia |
Synonyms |
Congenital hypotrichia (disorder)
Congenital hypotrichosis
Hypotrichosis congenita
|
Type | http://www.w3.org/2002/07/owl#Class |
All Properties
altLabel |
Congenital hypotrichia (disorder)
Congenital hypotrichosis
Hypotrichosis congenita
|
---|---|
prefLabel | Congenital hypotrichia
|
Type ID |
900000000000003001
900000000000013009
|
CASE SIGNIFICANCE ID | 900000000000448009
|
notation | 56558005
|
Effective time | 20200731
|
Active | 1
|
Has finding site | |
Has pathological process | |
subClassOf | |
Semantic type UMLS property | |
type | |
Subset member | 6011000124106~MAPTARGET~L81.4
6011000124106~MAPADVICE~ALWAYS Q84.0
6011000124106~MAPTARGET~Q15.9
447562003~MAPRULE~TRUE
6011000124106~MAPRULE~IFA 773625007 | Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome |
6011000124106~MAPTARGET~K05.30
6011000124106~MAPADVICE~IF NEONATAL SCLEROSING CHOLANGITIS, ICHTHYOSIS, HYPOTRICHOSIS SYNDROME CHOOSE K83.09 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPADVICE~IF LINEAR HYPOPIGMENTATION AND CRANIOFACIAL ASYMMETRY WITH ACRAL, OCULAR AND BRAIN ANOMALIES CHOOSE Q74.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPADVICE~IF LINEAR HYPOPIGMENTATION AND CRANIOFACIAL ASYMMETRY WITH ACRAL, OCULAR AND BRAIN ANOMALIES CHOOSE Q67.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPADVICE~IF HYPOTRICHOSIS WITH JUVENILE MACULAR DEGENERATION SYNDROME CHOOSE Q84.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPADVICE~IF SPONDYLOEPIMETAPHYSEAL DYSPLASIA, HYPOTRICHOSIS SYNDROME CHOOSE Q77.7 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPTARGET~F78.A9
6011000124106~MAPPRIORITY~7
6011000124106~MAPPRIORITY~4
6011000124106~MAPADVICE~IF SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, HYPOTRICHOSIS SYNDROME CHOOSE R62.52 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPADVICE~IF CONGENITAL ICHTHYOSIS WITH HYPOTRICHOSIS SYNDROME CHOOSE Q84.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA
6011000124106~MAPADVICE~IF SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, HYPOTRICHOSIS SYNDROME CHOOSE Q84.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPADVICE~IF HYPOTRICHOSIS, OSTEOLYSIS, PERIODONTITIS, PALMOPLANTAR KERATODERMA SYNDROME CHOOSE Q82.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPTARGET~Q87.0
447562003~MAPTARGET~Q84.0
6011000124106~MAPTARGET~
6011000124106~MAPCATEGORYID~447638001
6011000124106~MAPADVICE~IF HYPOTRICHOSIS WITH KERATOSIS PILARIS AND LENTIGINOSIS CHOOSE Q82.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPGROUP~1
6011000124106~MAPGROUP~2
6011000124106~MAPPRIORITY~10
6011000124106~MAPADVICE~IF HEREDITARY HYPOTRICHOSIS WITH RECURRENT SKIN VESICLES SYNDROME CHOOSE L98.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPPRIORITY~8
6011000124106~MAPTARGET~Q77.7
900000000000508004~ACCEPTABILITYID~900000000000549004
6011000124106~MAPADVICE~IF SPONDYLOEPIMETAPHYSEAL DYSPLASIA, HYPOTRICHOSIS SYNDROME CHOOSE Q84.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
447562003~MAPGROUP~1
6011000124106~MAPTARGET~F79
6011000124106~MAPADVICE~IF HYPOTRICHOSIS WITH JUVENILE MACULAR DEGENERATION SYNDROME CHOOSE H35.50 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPTARGET~Q82.8
447562003~CORRELATIONID~447561005
6011000124106~MAPADVICE~IF NEONATAL SCLEROSING CHOLANGITIS, ICHTHYOSIS, HYPOTRICHOSIS SYNDROME CHOOSE K83.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPTARGET~Q80.9
6011000124106~MAPCATEGORYID~447637006
900000000000509007~ACCEPTABILITYID~900000000000548007
6011000124106~MAPADVICE~ALWAYS Q84.0 | DESCENDANTS NOT EXHAUSTIVELY MAPPED
6011000124106~MAPRULE~IFA 254227008 | Hypotrichosis with keratosis pilaris and lentiginosis |
6011000124106~MAPADVICE~IF HYPOTRICHOSIS AND INTELLECTUAL DISABILITY SYNDROME LOPES TYPE CHOOSE F79 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPRULE~IFA 773300008 | Spondyloepimetaphyseal dysplasia, hypotrichosis syndrome |
6011000124106~MAPADVICE~IF SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, HYPOTRICHOSIS SYNDROME CHOOSE Q74.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPADVICE~IF LINEAR HYPOPIGMENTATION AND CRANIOFACIAL ASYMMETRY WITH ACRAL, OCULAR AND BRAIN ANOMALIES CHOOSE Q82.4 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPTARGET~Q74.9
900000000000508004~ACCEPTABILITYID~900000000000548007
6011000124106~MAPADVICE~IF HYPOTRICHOSIS AND INTELLECTUAL DISABILITY SYNDROME LOPES TYPE CHOOSE Q84.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPRULE~IFA 254227008 | Hypotrichosis with keratosis pilaris and lentiginosis (disorder) |
447562003~MAPADVICE~ALWAYS Q84.0
6011000124106~MAPTARGET~H35.50
6011000124106~MAPADVICE~IF HEREDITARY HYPOTRICHOSIS WITH RECURRENT SKIN VESICLES SYNDROME CHOOSE L65.9 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
447562003~MAPPRIORITY~1
6011000124106~MAPADVICE~IF HYPOTRICHOSIS, OSTEOLYSIS, PERIODONTITIS, PALMOPLANTAR KERATODERMA SYNDROME CHOOSE K05.30 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPTARGET~Q04.9
447562003~MAPCATEGORYID~447637006
6011000124106~MAPGROUP~5
6011000124106~MAPRULE~OTHERWISE TRUE
6011000124106~MAPPRIORITY~5
6011000124106~MAPADVICE~IF CONGENITAL ICHTHYOSIS WITH HYPOTRICHOSIS SYNDROME CHOOSE Q80.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPRULE~IFA 724350009 | Hereditary hypotrichosis with recurrent skin vesicles syndrome |
6011000124106~MAPGROUP~4
6011000124106~MAPPRIORITY~9
6011000124106~MAPADVICE~IF NEONATAL SCLEROSING CHOLANGITIS, ICHTHYOSIS, HYPOTRICHOSIS SYNDROME CHOOSE Q84.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPCATEGORYID~447639009
6011000124106~MAPTARGET~Q82.4
6011000124106~MAPRULE~IFA 1208985003 | Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies |
6011000124106~MAPRULE~IFA 724277002 | Congenital ichthyosis with hypotrichosis syndrome |
6011000124106~MAPRULE~IFA 724278007 | Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome |
6011000124106~MAPRULE~IFA 723365002 | Hypotrichosis and intellectual disability syndrome Lopes type |
6011000124106~MAPTARGET~R62.52
6011000124106~MAPADVICE~IF HYPOTRICHOSIS, OSTEOLYSIS, PERIODONTITIS, PALMOPLANTAR KERATODERMA SYNDROME CHOOSE M89.50 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPADVICE~IF SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, HYPOTRICHOSIS SYNDROME CHOOSE Q87.0 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPADVICE~IF HYPOTRICHOSIS WITH KERATOSIS PILARIS AND LENTIGINOSIS CHOOSE L81.4 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPPRIORITY~1
6011000124106~MAPADVICE~IF HYPOTRICHOSIS AND INTELLECTUAL DISABILITY SYNDROME LOPES TYPE CHOOSE F78.A9 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPTARGET~L65.9
6011000124106~MAPPRIORITY~6
6011000124106~MAPADVICE~IF LINEAR HYPOPIGMENTATION AND CRANIOFACIAL ASYMMETRY WITH ACRAL, OCULAR AND BRAIN ANOMALIES CHOOSE Q15.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~CORRELATIONID~447561005
6011000124106~MAPTARGET~M89.50
900000000000497000~MAPTARGET~X78Dg
6011000124106~MAPTARGET~L98.9
6011000124106~MAPTARGET~Q67.0
6011000124106~MAPTARGET~K83.09
6011000124106~MAPTARGET~Q74.8
6011000124106~MAPRULE~TRUE
6011000124106~MAPADVICE~IF LINEAR HYPOPIGMENTATION AND CRANIOFACIAL ASYMMETRY WITH ACRAL, OCULAR AND BRAIN ANOMALIES CHOOSE Q04.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPTARGET~Q84.0
6011000124106~MAPGROUP~3
6011000124106~MAPTARGET~K83.0
6011000124106~MAPPRIORITY~3
900000000000509007~ACCEPTABILITYID~900000000000549004
6011000124106~MAPADVICE~IF HYPOTRICHOSIS, OSTEOLYSIS, PERIODONTITIS, PALMOPLANTAR KERATODERMA SYNDROME CHOOSE Q84.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPPRIORITY~2
6011000124106~MAPRULE~IFA 763658004 | Hypotrichosis, osteolysis, periodontitis, palmoplantar keratoderma syndrome |
6011000124106~MAPRULE~IFA 723364003 | Hypotrichosis with juvenile macular degeneration syndrome |
6011000124106~MAPADVICE~IF NEONATAL SCLEROSING CHOLANGITIS, ICHTHYOSIS, HYPOTRICHOSIS SYNDROME CHOOSE Q80.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
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|
DEFINITION STATUS ID | 900000000000073002
|
tui | T019
|
CTV3ID | X78Dg
|
Occurs in | |
cui | C4721530
|
Has associated morphology |
Delete | Subject | Author | Type | Created |
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No notes to display |
- Problem retrieving properties:
Notes
Subject | Author | Type | Class | Created |
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ICD-10-CM 2018 | Certified+Professional+Coder+ | Comment | http://purl.bioontology.org/ontology/SNOMEDCT/40068008 | 2018-06-08 |
Surgical specialty should be surgury? | jimmccusker | Comment | http://purl.bioontology.org/ontology/SNOMEDCT/394732004 | 2012-09-26 |
SNOMEDCT | kotharu | Comment | http://purl.bioontology.org/ontology/SNOMEDCT/123037004 | 2012-04-17 |
Add NCBO Web Widgets to your site for SNOMEDCT
Widget type | Widget demonstration |
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Step 2: Follow the Instructions
For more help visit NCBO Widget Wiki |
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Example 1 (start typing the class name to get its full URI)
Example 2 (get the ID for a class) Example 3 (get the preferred name for a class) Step 2: Follow the Instructions
For more help visit NCBO Widget Wiki |
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Step 2: Follow the InstructionsCopy the code below and paste it to your HTML page <iframe frameborder="0" src="/widgets/visualization?ontology=SNOMEDCT&class=http%3A%2F%2Fpurl.bioontology.org%2Fontology%2FSNOMEDCT%2F1286952001&apikey=YOUR_API_KEY"></iframe> For more help visit NCBO Widget Wiki |
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Step 2: Follow the InstructionsCopy the code below and paste it to your HTML page <link rel="stylesheet" type="text/css" href="/widgets/jquery.ncbo.tree.css"> <script src="/widgets/jquery.ncbo.tree-2.0.2.js"></script> <div id="widget_tree"></div> var widget_tree = $("#widget_tree").NCBOTree({ apikey: "YOUR_API_KEY", ontology: "SNOMEDCT" }); You can also view a detailed demonstration For more help visit NCBO Widget Wiki |