grant syndrome

Preferred Label : grant syndrome;

MeSH note : Persistent wormian bones, blue sclerae, mandibular hypoplasia, shallow glenoid fossae and campomelia;

Details

Origin ID

C537293;

UMLS CUI

C1841835;

Currated CISMeF NLP mapping
- Grant syndrome [ICD-11 More detail]
- Grant syndrome [OMIM Phenotype]
- Grant syndrome [ORDO Disease]
- Grant syndrome (disorder) [SNOMED CT concept]
Has phenotype(s) (HPO)
- Sloping shoulders [HPO term]
MeSH term(s) associated for indexing
- abnormalities, multiple [MeSH Descriptor]
- craniofacial abnormalities [MeSH Descriptor]
- osteogenesis imperfecta [MeSH Descriptor]
ORDO relation(s)
- Grant syndrome [ORDO Disease]
Record concept(s)
- Grant syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Grant syndrome [ORDO Disease]
- Grant syndrome [OMIM Phenotype]
- Grant syndrome (disorder) [SNOMED CT concept]

Keyword's position in hierarchy(ies) :

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