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Q38413219-17909E0F-D99B-4B8D-9B1E-39B2F0B3B97D
Q38413219-17909E0F-D99B-4B8D-9B1E-39B2F0B3B97D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38413219-17909E0F-D99B-4B8D-9B1E-39B2F0B3B97D
Clinical utility gene card for: Mowat-Wilson syndrome
P2860
Q38413219-17909E0F-D99B-4B8D-9B1E-39B2F0B3B97D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38413219-17909E0F-D99B-4B8D-9B1E-39B2F0B3B97D
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Statement
wasDerivedFrom
90670b15639348d20ee52154556690e6ac4abcc7
P2860
Clinical features of a form of Hirschsprung's disease caused by a novel genetic abnormality.