Familial amyloid polyneuropathy, jewish type (disorder)
SCTID: 41590007, Primitive, Active
41590007 |Familial amyloid polyneuropathy, jewish type (disorder)|
2164018013 - Jewish type amyloid polyneuropathy (en) View
69376017 - Familial amyloid polyneuropathy, 33 Ile-for-Phe (en) View
69375018 - Familial amyloid polyneuropathy, Jewish type (en) View
778394014 - Familial amyloid polyneuropathy, Jewish type (disorder) (en) View
Relationship (3465500020) - 41590007 -> 3058005 (363698007) View
Relationship (6596117024) - 41590007 -> 84782009 (363698007) View
Relationship (12829195020) - 41590007 -> 84782009 (363698007) View
Relationship (776014023) - 41590007 -> 3057000 (363698007) View
Relationship (776012022) - 41590007 -> 3058005 (363698007) View
Relationship (776013028) - 41590007 -> 68790008 (116676008) View
Relationship (3454019029) - 41590007 -> 68790008 (116676008) View
Relationship (2461838020) - 41590007 -> 398229007 (116680003) View
Relationship (2547063026) - 41590007 -> 42295001 (116680003) View
Relationship (215886025) - 41590007 -> 42295001 (116680003) View
42295001 View
ExtendedMap object (ffd1a5e5-1a55-595a-8c98-8cba34db3468) View
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