Anemia due to intrinsic red cell abnormality (disorder)
SCTID: 323666000, Primitive, Active
323666000 |Anemia due to intrinsic red cell abnormality (disorder)|
465061011 - Anaemia due to intrinsic red cell abnormality (en) View
465062016 - Anemia due to intrinsic red cell abnormality (en) View
717606012 - Anemia due to intrinsic red cell abnormality (disorder) (en) View
Relationship (6765132025) - 323666000 -> 281300000 (363713009) View
Relationship (6765133024) - 323666000 -> 441689006 (363714003) View
Relationship (6765134029) - 323666000 -> 281300000 (363713009) View
Relationship (6765135028) - 323666000 -> 14089001 (363714003) View
Relationship (682039023) - 323666000 -> 41898006 (363698007) View
Relationship (2261900023) - 323666000 -> 62574001 (363705008) View
Relationship (2261899029) - 323666000 -> 57171008 (363698007) View
Relationship (682038026) - 323666000 -> 57171008 (363698007) View
Relationship (147514024) - 323666000 -> 271737000 (116680003) View
271737000 View
1963002 View
3272007 View
37272000 View
87994004 View
111575000 View
127040003 View
ExtendedMap object (624bd093-a457-515c-ba11-f456480ca332) View
ExtendedMap object (64a0b02f-9c48-5732-be5b-e76358a07621) View
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