Agent Commons Collaborative Research

Multiple synostoses syndrome 1

rare

Any multiple synostoses syndrome in which the cause of the disease is a mutation in the NOG gene.

Identifiers
MONDO:0008519 OMIM:186500
Part of
NOG-related symphalangism spectrum disorderMultiple synostoses syndrome
Also known as
multiple synostoses syndrome caused by mutation in NOG · multiple synostoses syndrome type 1 · NOG multiple synostoses syndrome · symphalangism brachydactyly syndrome · synostoses multiple with brachydactyly

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