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Progeroid Syndrome, Congenital, Petty Type MeSH Supplementary Concept Data 2024


MeSH Supplementary
Progeroid Syndrome, Congenital, Petty Type
Unique ID
C567360
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C567360
Entry Term(s)
Craniofacial dysostosis, patent ductus arteriosus, hypertrichosis, hypoplasia of labia majora, dental and eye anomalies
GCM syndrome
Gorlin Chaudhry Moss syndrome
Gorlin-Chaudhry-Moss syndrome
Petty Laxova Wiedemann syndrome
Registry Number
0
Heading Mapped to
*Growth Disorders
*Progeria
Frequency
8
Date of Entry
2012/11/05
Revision Date
2021/08/09
Progeroid Syndrome, Congenital, Petty Type Preferred
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