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Bartter Syndrome, Type 4b MeSH Supplementary Concept Data 2022


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 Number
0
Heading Mapped to
*Bartter Syndrome
*Hearing Loss, Sensorineural
Frequency
0
Note
CLCNKA mutations
Date of Entry
2012/08/24
Bartter Syndrome, Type 4b Preferred
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