deafness oligodontia syndrome

Preferred Label : deafness oligodontia syndrome;

MeSH note : Autosomal recessive sensorineural hearing impairment, dizziness, and hypodontia;

MeSH synonym : congenital profound sensorineural deafness and oligodontia; autosomal recessive sensorineural hearing impairment, dizziness, and hypodontia; Deafness-Oligodontia syndrome;

Details

Origin ID

C538049;

UMLS CUI

C1857333;

Automatic exact mappings (from CISMeF team)
- Deafness - oligodontia [ICD-11 More detail]
Currated CISMeF NLP mapping
- Deafness and oligodontia syndrome (disorder) [SNOMED CT concept]
- Deafness-oligodontia syndrome [OMIM Phenotype]
- Deafness-oligodontia syndrome [ORDO Disease]
Has phenotype(s) (HPO)
- Congenital sensorineural deafness [HPO term]
MeSH term(s) associated for indexing
- anodontia [MeSH Descriptor]
- hearing loss, sensorineural [MeSH Descriptor]
ORDO relation(s)
- Deafness-oligodontia syndrome [ORDO Disease]
Record concept(s)
- Deafness oligodontia syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Deafness and oligodontia syndrome (disorder) [SNOMED CT concept]
- Deafness-oligodontia syndrome [ORDO Disease]
- Deafness-oligodontia syndrome [OMIM Phenotype]

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