hereditary disease, nos

Preferred Label : hereditary disease, nos;

Details

Origin ID

DF-00180;

UMLS CUI

C0019247;

Automatic exact mappings (from CISMeF team)
- Ghost sickness (disorder) [SNOMED CT concept]
- Lethal congenital contracture syndrome type 1 (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Genetic Disorder [NCIt concept]
- Genetic disease [PASCAL descriptor]
- Genetic disease (disorder) [SNOMED CT concept]
- Genetic diseases [LOINC component]
- Genetic disorders [HPMULTI term]
- Genetic.Disorders [LOINC component]
- Hereditary disease [PASCAL descriptor]
- Hereditary disease (disorder) [SNOMED CT concept]
- Hereditary disorder [MedDRA Preferred Term]
- Hereditary disorder NOS [MedDRA LLT]
- genetic disease [DO Concept]
- genetic diseases, inborn [MeSH Descriptor]
- genetic disorder [Disease (Nov.)]
- genetic disorders [MedlinePlus Topic]
- hereditary disease [Artificial nutrition thesaurus concept]
- hereditary diseases [MeSH concept]
ICD-10 exact mapping(s)
- Unknown and unspecified causes of morbidity [ICD-10 category (who)]
SNOMED CT concept
- Hereditary disease (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Genetic Disorder [NCIt concept]
- Genetic disease (disorder) [SNOMED CT concept]
- Genetic diseases [LOINC component]
- Genetic syndrome (disorder) [Inactive SNOMED CT concept]
- Genetic.Disorders [LOINC component]
- Hereditary disease (disorder) [SNOMED CT concept]
- Hereditary disorder [MedDRA Preferred Term]
- Hereditary disorder NOS [MedDRA LLT]
- genetic disease [DO Concept]
- genetic disorders [MedlinePlus Topic]
- hereditary diseases [MeSH concept]
Validated automatic mappings to BTNT
- inborn genetic disorder [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

Main resources

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