otodental dysplasia

Preferred Label : otodental dysplasia;

MeSH synonym : chromosome 11q13 deletion syndrome; otodental syndrome;

Related MeSH term : Otodental Syndrome With Coloboma;

Details

Origin ID

C563482;

UMLS CUI

C1833693;

Currated CISMeF NLP mapping
- Otodental dysplasia [OMIM Phenotype]
- Otodental syndrome [ORDO Disease]
- Otodental syndrome (disorder) [SNOMED CT concept]
MeSH term(s) associated for indexing
- chromosome deletion [MeSH Descriptor]
- chromosome disorders [MeSH Descriptor]
- chromosomes, human, pair 11 [MeSH Descriptor]
- coloboma [MeSH Descriptor]
- hearing loss, sensorineural [MeSH Descriptor]
- tooth abnormalities [MeSH Descriptor]
Record concept(s)
- oculootodental syndrome [MeSH concept]
- otodental dysplasia [MeSH concept]
See also inter- (CISMeF)
- Oculootodental syndrome [ORDO Disease]
- oculootodental syndrome [Disease (Nov.)]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Otodental dysplasia [OMIM Phenotype]
- Otodental syndrome [ORDO Disease]
- Otodental syndrome (disorder) [SNOMED CT concept]

Keyword's position in hierarchy(ies) :

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