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Chromosome 6pter-P24 Deletion Syndrome MeSH Supplementary Concept Data 2022


MeSH Supplementary
Chromosome 6pter-P24 Deletion Syndrome
Unique ID
C567239
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C567239
Registry Number
0
Heading Mapped to
*Chromosome Deletion
Chromosomes, Human, Pair 6
*Eye Abnormalities
*Heart Defects, Congenital
*Hypertelorism
*Hearing Loss
Frequency
3
Date of Entry
2012/11/05
Chromosome 6pter-P24 Deletion Syndrome Preferred
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