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Q37715520-F979E46F-9BBC-432F-8A13-635CF6906B8E
Q37715520-F979E46F-9BBC-432F-8A13-635CF6906B8E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37715520-F979E46F-9BBC-432F-8A13-635CF6906B8E
PMP22 related neuropathies: Charcot-Marie-Tooth disease type 1A and Hereditary Neuropathy with liability to Pressure Palsies.
P2860
Q37715520-F979E46F-9BBC-432F-8A13-635CF6906B8E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37715520-F979E46F-9BBC-432F-8A13-635CF6906B8E
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wasDerivedFrom
c556052aa0605cbf34a579f769e562bcc7f16e17
P2860
Peripheral myelin protein-22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot-Marie-Tooth 1A.