Greig cephalopolysyndactyly syndrome

Orpha code: 380OMIM code: 175700

Definition

A rare developmental defect during embryogenesis with digit duplication, polydactyly, syndactyly, and/or hyperphalangy characterized by multiple congenital anomaly syndrome.

Disease data
Classification

Malformation syndrome

Synonyms
GCPS
GCPS
ORPHA code
380
OMIM code
175700
ICD10 code
Q87.0
ICD11 code
LD26.2

No additional description.

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