Congenital hypoplasia (morphologic abnormality)
SCTID: 38146002, Primitive, Inactive
38146002 |Congenital hypoplasia (morphologic abnormality)|
64768019 - Congenital hypoplasia (en) View
771355019 - Congenital hypoplasia (morphologic abnormality) (en) View
64774019 - Incomplete development (en) View
64773013 - Rudimentary structure (en) View
64775018 - Underdevelopment (en) View
64769010 - Congenital hypoplasia, NOS (en) View
64771010 - Incomplete development, NOS (en) View
64770011 - Rudimentary structure, NOS (en) View
64772015 - Underdevelopment, NOS (en) View
Relationship (209976027) - 38146002 -> 55199003 (116680003) View
Relationship (2007491020) - 38146002 -> 112635002 (116680003) View
Relationship (209977020) - 38146002 -> 107656002 (116680003) View
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