Trisomy 10p

Orpha code: 171929OMIM code:

Definition

Trisomy 10p is a syndrome of mental retardation/multiple congenital malformations (MR-MCA) that is caused by the total or partial duplication of the short arm of chromosome 10.

Disease data
Classification

Malformation syndrome

ORPHA code
171929
OMIM code
-
ICD10 code
Q92.2
ICD11 code
-

No additional description.

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