OMOP Concept 443916
Hereditary disease
StandardConditionSNOMED32895009Disorder
Maps from
4
Descendants
4,928
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
4 source codes normalize to Hereditary disease via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 138779 | Hereditary epistaxis | Non-standard |
| CIEL | 150739 | Abortive cerebellar ataxia | Non-standard |
| ICD10CM | I67.858 | Other hereditary cerebrovascular disease | Non-standard |
| MeSH | D030342 | Genetic Diseases, Inborn | Non-standard |
Synonyms
Alternative names recorded for Hereditary disease across source vocabularies.
- enfermedad heredada
- enfermedad hereditaria
- enfermedad hereditaria (trastorno)
- Hereditary disease (disorder)
- Inherited disease
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(3)Roll up to these when you need a wider cohort.
Narrower concepts
(4,928)Included automatically when you query with descendants.
- 1Autosomal hereditary disorder
- 1Chronic granulomatous disease
- 1Connective tissue hereditary disorder
- 1Developmental hereditary disorder
- 1Familial hemorrhagic diathesis
- 1Familial juvenile hypertrophy of breast
- 1Familial thyroglossal duct cyst
- 1Fetal hereditary disease
- 1Hereditary amyloidosis
- 1Hereditary angioedema
- 1Hereditary cancer-predisposing syndrome
- 1Hereditary coagulation factor deficiency
- 1Hereditary disorder by system
- 1Hereditary dysplasminogenemia
- 1Hereditary folate deficiency anemia
- 1Hereditary hypoplasminogenemia
- 1Hereditary iron deficiency anemia
- 1Hereditary metabolic disease
- 1Hereditary thrombophilia
- 1Hereditary vasopressin-related polyuria
- 1Hereditary vitamin B12 deficiency anemia
- 1Isolated agammaglobulinemia
- 1Maternally inherited mitochondrial deoxyribonucleic acid disease
- 1Mendelian disorders
- 1Mendelian susceptibility to mycobacterial disease
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