Disease: Hydrops Fetalis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0020305
Disease: Hydrops Fetalis
Hydrops Fetalis 		0.010 GeneticVariation disease BEFREE A 3-bp deletion mutation of PTPN11 in an infant with severe Noonan syndrome including hydrops fetalis and juvenile myelomonocytic leukemia. 15211660 2004