Dentin dysplasia with sclerotic bones - CISMeF

" /> Dentin dysplasia with sclerotic bones - CISMeF

CISMeF

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Dentin dysplasia with sclerotic bonesOMIM Phenotype

Preferred Label : Dentin dysplasia with sclerotic bones;

Type : Phenotype or locus, molecular basis unknown;

Inheritance : Autosomal dominant;

Prefixed ID : %125440;

Details

Origin ID

125440;

UMLS CUI

C1852201;

Broader ORDO disease(s)
- Dentin dysplasia [ORDO Disease]
Currated CISMeF NLP mapping
- Dentin dysplasia sclerotic bones [MeSH concept]
- Dentin dysplasia with sclerotic bone syndrome (disorder) [SNOMED CT concept]
- Dentin dysplasia-sclerotic bones syndrome [ORDO Disease]
- dentin dysplasia sclerotic bones [MeSH Supplementary Concept]
HPO term(s)
- Abnormality of the dentition [HPO term]
- Autosomal dominant inheritance [HPO term]
- Cortical sclerosis [HPO term]
- Dentinogenesis imperfecta limited to primary teeth [HPO term]
ORDO concept(s)
- Dentin dysplasia-sclerotic bones syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Dentin dysplasia sclerotic bones [MeSH concept]
- Dentin dysplasia-sclerotic bones syndrome [ORDO Disease]
- dentin dysplasia sclerotic bones [MeSH Supplementary Concept]

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02/05/2025

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