Granular cell hypoplasia (disorder)
SCTID: 253178001, Primitive, Active
253178001 |Granular cell hypoplasia (disorder)|
377074015 - Granular cell hypoplasia (en) View
643906015 - Granular cell hypoplasia (disorder) (en) View
Relationship (4972030028) - 253178001 -> 255399007 (246454002) View
Relationship (5003967021) - 253178001 -> 55199003 (116676008) View
Relationship (5003968027) - 253178001 -> 25991003 (363698007) View
Relationship (6125399024) - 253178001 -> 55199003 (116676008) View
Relationship (6125400028) - 253178001 -> 255399007 (246454002) View
Relationship (6125401029) - 253178001 -> 25991003 (363698007) View
Relationship (10526735023) - 253178001 -> 308490002 (370135005) View
Relationship (73009021) - 253178001 -> 253171007 (116680003) View
Relationship (568588028) - 253178001 -> 255399007 (246454002) View
Relationship (3431588025) - 253178001 -> 107656002 (116676008) View
Relationship (3431589022) - 253178001 -> 113305005 (363698007) View
Relationship (5003966028) - 253178001 -> 16026008 (116680003) View
Relationship (3257305027) - 253178001 -> 107656002 (116676008) View
Relationship (3257306026) - 253178001 -> 113305005 (363698007) View
Relationship (568589020) - 253178001 -> 113305005 (363698007) View
Relationship (3207130027) - 253178001 -> 371519002 (116676008) View
Relationship (2578733023) - 253178001 -> 107656002 (116676008) View
Relationship (2715377025) - 253178001 -> 25087005 (363698007) View
Relationship (2715378024) - 253178001 -> 21390004 (116676008) View
16026008 View
ExtendedMap object (71b87b51-3adf-5127-b62d-8f67618a2b54) View
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