progeroid syndrome, congenital, petty type

Preferred Label : progeroid syndrome, congenital, petty type;

MeSH synonym : Gorlin Chaudhry Moss syndrome; GCM syndrome; Gorlin-Chaudhry-Moss syndrome; Petty Laxova Wiedemann syndrome; Craniofacial dysostosis, patent ductus arteriosus, hypertrichosis, hypoplasia of labia majora, dental and eye anomalies;

Details

Origin ID

C567360;

UMLS CUI

C2676780;

Automatic exact mappings (from CISMeF team)
- Progeroid syndrome Petty type (disorder) [SNOMED CT concept]
- Progeroid syndrome, Petty type [ORDO Disease]
Currated CISMeF NLP mapping
- Fontaine progeroid syndrome [OMIM Phenotype]
MeSH term(s) associated for indexing
- growth disorders [MeSH Descriptor]
- progeria [MeSH Descriptor]
Record concept(s)
- progeroid syndrome, congenital, petty type [MeSH concept]
See also inter- (CISMeF)
- Gorlin-Chaudhry-Moss syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Fontaine progeroid syndrome [OMIM Phenotype]
- Gorlin-Chaudhry-Moss syndrome (disorder) [SNOMED CT concept]
- Progeroid syndrome Petty type (disorder) [SNOMED CT concept]

Keyword's position in hierarchy(ies) :

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