Hyperimmunoglobulin m syndrome type 3 (disorder)
SCTID: 1362020006, Primitive, Active
1362020006 |Hyperimmunoglobulin m syndrome type 3 (disorder)|
5443856010 - Autosomal recessive combined immunodeficiency due to CD40 mutation (en) View
5443853019 - HIGM3 - hyperimmunoglobulin M syndrome type 3 (en) View
5443854013 - Hyper-IgM syndrome due to CD40 deficiency (en) View
5443852012 - Hyperimmunoglobulin M syndrome type 3 (en) View
5443855014 - Hyperimmunoglobulin M syndrome type 3 (disorder) (en) View
Relationship (16315434024) - 1362020006 -> 403836001 (116680003) View
Relationship (16315435020) - 1362020006 -> 783248004 (116680003) View
Relationship (16315436021) - 1362020006 -> 769247005 (370135005) View
403836001 View
783248004 View
ExtendedMap object (f95bf200-0fe1-5e11-b3cc-d1213fcbc475) View
No recent searches