OMOP Concept 437256
Hereditary factor XI deficiency disease
StandardConditionSNOMED49762007Disorder
Maps from
16
Descendants
3
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
16 source codes normalize to Hereditary factor XI deficiency disease via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 117578 | Congenital factor XI deficiency | Non-standard |
| CIM10 | D68.1 | Hereditary factor XI deficiency | Non-standard |
| ICD10 | D68.1 | Hereditary factor XI deficiency | Non-standard |
| ICD10CM | D68.1 | Hereditary factor XI deficiency | Non-standard |
| ICD10CN | D68.1 | Hereditary factor XI deficiency | Non-standard |
| ICD10CN | D68.100 | Hereditary factor XI deficiency | Non-standard |
| ICD10CN | D68.101 | Hemophilia C type (machine translation) | Non-standard |
| ICD10GM | D68.1 | Hereditary factor XI deficiency | Non-standard |
| ICD9CM | 286.2 | Congenital factor XI deficiency | Non-standard |
| KCD7 | D68.1 | Hereditary factor ? deficiency | Non-standard |
| MeSH | D005173 | Factor XI Deficiency | Non-standard |
| Nebraska Lexicon | 49762007 | Factor XI deficiency | Non-standard |
| OXMIS | 2862 | FACTOR XI DEFICIENCY | Non-standard |
| Read | D302.00 | Haemophilia-C (factor XI deficiency) | Non-standard |
| Read | D302.11 | Haemophilia C | Non-standard |
| Read | D302.12 | Rosenthal's disease | Non-standard |
Synonyms
Alternative names recorded for Hereditary factor XI deficiency disease across source vocabularies.
- Congenital factor XI deficiency disease
- deficiencia congénita de factor XI
- deficiencia del antecedente de la tromboplastina plasmática
- deficiencia hereditaria de factor XI
- deficiencia hereditaria de factor XI (trastorno)
- enfermedad de Rosenthal
- Haemophilia C
- hemofilia C
- Hemophilia C
- Hereditary factor XI deficiency disease (disorder)
- Plasma thromboplastin antecedent deficiency
- PTA deficiency
- Rosenthal's disease
- Thromboplastin antecedent deficiency
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(17)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Congenital disease
- 1Contact factor deficiency
- 1Factor XI deficiency
- 1Hemophilia
- 2Autosomal hereditary disorder
- 2Blood coagulation disorder
- 2Coagulation factor deficiency syndrome
- 2Disorder of fetus and/or newborn
- 3Disease
- 3Disorder of hemostatic system
- 3Hereditary disease
- 3OMOP Bleeding 1
- 3OMOP Bleeding 2
- 4Clinical finding
- 4Functional finding
- 4Genetic disease
Narrower concepts
(3)Included automatically when you query with descendants.
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