Congenital hyperpigmentation (morphologic abnormality)
SCTID: 56588001, Primitive, Inactive
56588001 |Congenital hyperpigmentation (morphologic abnormality)|
94104017 - Congenital hyperpigmentation (en) View
795116010 - Congenital hyperpigmentation (morphologic abnormality) (en) View
Relationship (240175022) - 56588001 -> 62307005 (116680003) View
Relationship (5972806022) - 56588001 -> 4830009 (116680003) View
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