deafness, autosomal recessive 1b

Preferred Label : deafness, autosomal recessive 1b;

MeSH synonym : DFNB1B;

Origin ID

C567213;

UMLS CUI

C2675235;

Currated CISMeF NLP mapping
- Deafness, autosomal recessive 1b [OMIM Phenotype]
- autosomal recessive nonsyndromic deafness 1B [DO Concept]
MeSH term(s) associated for indexing
- hearing loss, sensorineural [MeSH Descriptor]
Record concept(s)
- deafness, autosomal recessive 1b [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Deafness, autosomal recessive 1b [OMIM Phenotype]