deafness, autosomal recessive 3

Preferred Label : deafness, autosomal recessive 3;

MeSH synonym : neurosensory nonsyndromic recessive deafness 3;

Origin ID

C563961;

UMLS CUI

C1838263;

CISMeF manual mappings
- nonsyndromic sensorineural deafness autosomal recessive 3 [Disease (Nov.)]
Currated CISMeF NLP mapping
- Deafness, autosomal recessive 3 [OMIM Phenotype]
- autosomal recessive nonsyndromic deafness 3 [DO Concept]
MeSH term(s) associated for indexing
- hearing loss, sensorineural [MeSH Descriptor]
Record concept(s)
- deafness, autosomal recessive 3 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Deafness, autosomal recessive 3 [OMIM Phenotype]
- autosomal recessive nonsyndromic deafness 3 [DO Concept]
- nonsyndromic sensorineural deafness autosomal recessive 3 [Disease (Nov.)]