Autosomal recessive limb girdle muscular dystrophy type 2p (disorder)
SCTID: 726614009, Primitive, Active
726614009 |Autosomal recessive limb girdle muscular dystrophy type 2p (disorder)|
3450986014 - Autosomal recessive limb girdle muscular dystrophy type 2P (en) View
3450985013 - Autosomal recessive limb girdle muscular dystrophy type 2P (disorder) (en) View
Relationship (11283815029) - 726614009 -> 308490002 (370135005) View
Relationship (11570422025) - 726614009 -> 255314001 (263502005) View
Relationship (6930977023) - 726614009 -> 240054004 (116680003) View
Relationship (6930978029) - 726614009 -> 4720007 (116676008) View
Relationship (6930979021) - 726614009 -> 127954009 (363698007) View
240054004 View
ExtendedMap object (c8f2ac9c-debd-58d3-bbfb-d6cf8d1ef185) View
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