Taurodontism - CISMeF

Preferred Label : Taurodontism;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : likely polygenic; ? Autosomal recessive;

Prefixed ID : 272700;

Details

Origin ID

272700;

UMLS CUI

C0266039;

Automatic exact mappings (from CISMeF team)
- Taurodontia [HRDO Sign]
- Taurodontism [ICD-11 More detail]
Currated CISMeF NLP mapping
- Abnormalities of size and form of teeth [ICD-10 Sub-category]
- Abnormalities of size and form of teeth [ICD-10 Sub-category (who)]
- Taurodontia [HPO term]
- Taurodontism [MeSH concept]
- Taurodontism [ORDO Disease]
- Taurodontism (disorder) [SNOMED CT concept]
- taurodontism [MeSH Supplementary Concept]
- taurodontism [SNOMED Notion]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Taurodontia [HPO term]
ORDO concept(s)
- Taurodontism [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Abnormalities of size and form of teeth [ICD-10 Sub-category (who)]
- Taurodontia [HPO term]
- Taurodontism [ORDO Disease]
- Taurodontism [MeSH concept]
- Taurodontism [MedDRA Preferred Term]
- Taurodontism (disorder) [SNOMED CT concept]
- taurodontism [MeSH Supplementary Concept]
- taurodontism [SNOMED Notion]

Keyword's position in hierarchy(ies) :

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