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Opitz GBBB Syndrome, X-Linked MeSH Supplementary Concept Data 2024


MeSH Supplementary
Opitz GBBB Syndrome, X-Linked
Unique ID
C567932
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C567932
Entry Term(s)
Opitz BBBG Syndrome, Type I
Opitz GBBB Syndrome, Type I
Opitz Syndrome
Opitz Syndrome, X-Linked
Opitz-G Syndrome, Type I
X-Linked Opitz Syndrome (XLOS)
Registry Number
0
Heading Mapped to
*Cleft Palate
Esophagus / *abnormalities
*Hypertelorism
*Hypospadias
*Genetic Diseases, X-Linked
Frequency
14
Date of Entry
2012/11/05
Revision Date
2013/10/24
Opitz GBBB Syndrome, X-Linked Preferred
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