MeSH Browser

MeSH Supplementary: Microtia, meatal atresia and conductive deafness
Unique ID: C537469
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537469
Entry Term(s): Familial microtia and meatal atresia; Familial microtia with meatal atresia and conductive deafness; Gupta Patton syndrome; Microtia meatal atresia deafness dominant; Microtia with meatal atresia and conductive deafness
Registry Numbers: 0
Heading Mapped to: Ear Canal / abnormalities; *Hearing Loss, Conductive; *Congenital Microtia
Frequency: 0
Date of Entry: 2010/08/25
Revision Date: 2014/08/08

Microtia, meatal atresia and conductive deafness MeSH Supplementary Concept Data 2025