Disease

Hydrops Fetalis

About the Disease
Lymphatic Malformation 7, also known as central conduction lymphatic anomaly, is related to lymphatic malformation 12 and autism spectrum disorder, and has symptoms including edema and peau d'orange. An important gene associated with Lymphatic Malformation 7 is EPHB4 (EPH Receptor B4). The drug Anti-Arrhythmia Agents has been mentioned in the context of this disorder. Affiliated tissues include lung, respiratory system-lung and respiratory system, and related phenotypes are anemia and atrial septal defect

Common Targets
SH3PXD2A | RRP12 | RASA1 | CYP2C19 | THSD1 | SPTA1 | DOK7 | EPHB4 | TECTB | PIEZO1 | ANGPT2 | LOXL4 | FOXC2 | GLDN | PTPN11 | PYROXD2

疾病靶点研报
Hydrops Fetalis

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