Greig cephalopolysyndactyly syndrome

Preferred Label : Greig cephalopolysyndactyly syndrome;

ICD-11 definition : Greig cephalopolysyndactyly syndrome is a pleiotropic, multiple congenital anomaly syndrome characterized by hypertelorism, macrocephaly with frontal bossing, and polysyndactyly most commonly preaxial in the feet and postaxial in the hands.;

Details

Origin ID

606500237;

Automatic exact mappings (from CISMeF team)
- Greig Syndrome [NCIt concept]
- Greig cephalopolysyndactyly syndrome [OMIM Phenotype]
- Greig cephalopolysyndactyly syndrome [DO Concept]
- Greig cephalopolysyndactyly syndrome [MeSH concept]
- Greig cephalopolysyndactyly syndrome [ORDO Disease]
- Greig cephalopolysyndactyly syndrome (disorder) [SNOMED CT concept]
- Greig's syndrome [MedDRA Preferred Term]
- greig cephalopolysyndactyly syndrome [MeSH Supplementary Concept]
- greig cephalopolysyndactyly syndrome [SNOMED Notion]

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