Bartter Syndrome, Type 4b MeSH Supplementary Concept Data 2025

Details
Concepts

MeSH Supplementary: Bartter Syndrome, Type 4b
Unique ID: C567762
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567762
Entry Term(s): Bartter Syndrome, Infantile, with Sensorineural Deafness
Registry Numbers: 0
Heading Mapped to: *Bartter Syndrome; *Hearing Loss, Sensorineural
Frequency: 0
Note: CLCNKA mutations
Date of Entry: 2012/08/24
Revision Date: 1955/01/01

Bartter Syndrome, Type 4b Preferred

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