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Terminology chevron_right Concepts chevron_right 56588001

Production
The component that hold information about this concept.
Congenital hyperpigmentation (morphologic abnormality)
Congenital hyperpigmentation
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Congenital hyperpigmentation (morphologic abnormality)

SCTID: 56588001, Primitive, Inactive


56588001|Congenital hyperpigmentation (morphologic abnormality)|
  • en Congenital hyperpigmentation
  • en Congenital hyperpigmentation (morphologic abnormality)

56588001 |Congenital hyperpigmentation (morphologic abnormality)|

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